lzic[All Fields] AND 1[has_clinical] - dbVar - NCBI

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1.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: MIR5697; NMNAT1; TMEM274P; LZIC; RN7SKP269

Location information:

Clinical significance:

ID:: 48433886

variant

2.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: NMNAT1; MIR5697; TMEM274P; LZIC; RN7SKP269

Location information:

Clinical significance:

ID:: 53674442

variant

3.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: RN7SKP269; LZIC; MIR5697; NMNAT1; TMEM274P

Location information:

Clinical significance:

ID:: 53674583

variant

4.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: RPL9P11; FAM131C2P; PRAMEF9; RNU6-991P; PEX10; LOC105376689; PRAMEF20; KAZN; RPS16P1; CDK11B; TRN-GTT5-1; ICMT; HES4; MIIP; RNU6-304P; UTS2; ENO1; LOC105376686; LOC105378601; PRAMEF12; ATP13A2; MIR34A; PERM1; MIR6808; H6PD; LOC112267871; MIR200A; LOC112268220; MST1L; LOC107984918; PRKCZ-AS1; PIK3CD-AS2; CFL1P6; PLEKHG5; LINC01770; LINC01772; GPR157; MMEL1; PUSL1; LOC105378598; ATAD3B; RNU1-8P; ACOT7; CPTP; SPATA21; TAS1R1; RSC1A1; CCDC27; RPL23AP89; AJAP1; TNFRSF4; TNFRSF14-AS1; SSU72; RN7SL731P; TMEM201; LOC107984904; LINC02606; RPL26P7; HNRNPCL1; RNU1-1; KLHL17; C1orf127; ZBTB48; TRN-GTT13-1; PRAMEF2; ACTRT2; KCNAB2; RPL27P3; RPL12P14; LOC100288175; MASP2; MIR4689; PLEKHM2; PLOD1; PRAMEF32P; UBIAD1; TRN-GTT4-1; MIR4251; CHD5; GABRD; SNORD128; RNU6-731P; EXOSC10; RPL7P11; TNFRSF8; GNB1-DT; HES5; PDE4DIPP9; LOC105376805; NPPB; MMEL1-AS1; LOC105378600; RPL10P17; LOC112268219; PRAMEF13; MIR6729; UQCRHL; LOC105376682; HES3; RN7SL574P; CROCCP4; RNU6-1072P; FBXO6; MTHFR; RER1; LOC105376808; MRPL20; C1orf174; RNU1-7P; AADACL4; TMEM51; LINC01784; THAP3; LOC107985736; TRG-CCC4-1; RNU6ATAC18P; SCNN1D; EFHD2; EPHA2-AS1; LOC107984909; PRAMEF17; TRG-CCC1-1; LOC105378606; LOC100129381; AGRN; LOC107985467; RNU1-6P; LINC01346; LOC105378586; SLC25A33; AURKAIP1; MIR5697; LOC105376691; CALML6; HSPB7; MIR6730; PRDM16-DT; TTLL10; LINC01777; SMIM1; VWA1; UBE2J2; CPLANE2; CEP104; DFFA; LINC02593; SPSB1; LOC100129776; PLCH2; GPR153; RNF207; PRDM2; MIR6726; PDPN; C1orf167; RPL39P12; TMEM52; PLEKHN1; LINC01714; CAMTA1-AS2; CCNL2; PRAMEF10; TMEM240; LOC105378602; TAS1R3; TRE-TTC4-1; PDE4DIPP8; PRAMEF18; CROCCP3; RPL22; FBXO2; LOC105376733; MORN1; PIK3CD-AS1; C1orf159; LOC105378605; DNAJC16; RNU7-179P; LINC01647; RNU6-37P; RN7SL657P; NPPA; MRPL20-AS1; ZBTB2P1; ANKRD65-AS1; MFAP2; MTCYBP45; MIR200B; PGAM1P11; ZBTB17; EIF1AXP1; WRAP73; LRRC47; ATAD3C; CLSTN1; SLC25A34; HMGN2P17; FAM131C; PRAMEF14; RBP7; TRV-CAC13-1; CASP9; CTRC; RPL23AP19; DHRS3; LOC105378599; AADACL3; LOC107985732; RPL37P9; MIR4632; RPL39P6; MIR34AHG; SBF1P2; ANKRD65; UBE4B; MTOR-AS1; MIR6728; MMP23A; RN7SL451P; RNU6-291P; PIK3CD; PANK4; PHF13; ICMT-DT; CA6; SDF4; ISG15; VAMP3; CTNNBIP1; TRV-CAC11-1; LOC105378608; PRAMEF27; MFFP1; LOC107984911; RPL21P21; LINC01786; ARHGEF16; LOC105376756; SDHB; LOC105376739; LNCTAM34A; EXOSC10-AS1; FBLIM1; LINC02780; KIAA2013; KIF1B; LINC01672; EFHD2-AS1; LOC284600; PRAMEF6; RERE; PRAMEF15; TBCAP2; CAMTA1-DT; MIR551A; PRKCZ-DT; LOC105376759; SNORD167; LINC01646; CROCC; NOC2L; SPEN-AS1; KAZN-AS1; NECAP2; LOC107985469; CAMTA1; MEGF6; INTS11; PRAMEF8; SLC45A1; HNRNPCL4; ESPNP; PARK7; B3GALT6; TRG-CCC5-1; CASZ1; TMEM82; MST1P2; RNA5SP41; LOC105376712; MIR6727; LINC02783; MMP23B; CORT; TMEM51-AS1; TRE-TTC3-1; RN7SL614P; SRARP; CENPS; LOC100996583; LOC105376735; PEX14; SLC35E2B; MZT1P1; PER3; LOC105378604; EPHA2; LOC102724856; LINC01783; LOC105376695; TP73-AS3; PRAMEF34P; NPPA-AS1; ESPN; TNFRSF1B; TRUND-NNN4-1; TRV-CAC11-2; PRKCZ; HSPE1P24; ANO7L1; FHAD1; GNB1; RNU1-5P; ERRFI1; RNA5SP40; PRAMEF19; RNF223; PRAMEF35P; PRAMEF31P; FBXO42; CLCN6; RNU6-537P; SLC25A34-AS1; LOC101056699; MIR4252; LINC01345; LRRC38; RPL7P7; RNU6-771P; MAD2L2; PRAMEF36P; CLCNKB; PRAMEF7; MXRA8; DFFB; HNRNPCL3; NPHP4; SAMD11; RNU1-2; RN7SKP269; TMEM274P; FHAD1-AS1; ARHGEF19; LOC105378590; TPRG1L; PRAMEF5; PRDM16; GFOD3P; LOC100129534; RNU1-4; CENPS-CORT; CHCHD2P6; NBPF1; TNFRSF9; FBXO44; PRAMEF29P; LOC105378593; UBE2V2P3; PRAMEF11; LINC02766; LOC101060126; RNF207-AS1; PRAMEF28P; SLC2A5; LOC112268261; C1QTNF12; LOC105378948; PRAMEF1; MT1XP1; CROCCP2; RPL22P3; TARDBP; LOC100420339; LOC105376767; LOC112268218; TTLL10-AS1; DNAJC11; NDUFB4P8; MFN2; C1orf167-AS1; CFAP107; ACAP3; RNU6-1265P; AGMAT; LINC02782; LZIC; LOC107984913; DVL1; NMNAT1; HNRNPCL2; LINC01342; PRAMEF26; RNU5E-4P; RNU6-777P; TNFRSF18; SNORA59A; TTC34; LOC107985101; TNFRSF14; PRAMEF4; DRAXIN; RNU5E-1; PRAMEF30P; SCARNA21B; VPS13D; LOC107984872; LOC105376674; RNU1-3; MIR3675; LOC105378589; CD24P1; EEF1DP6; PRAMEF33; BRWD1P1; TMEM51-AS2; PADI2; ATAD3A; LOC107985729; TRG-CCC1-2; LOC107984912; CAMTA1-AS1; ENO1-AS1; LINC02781; ANGPTL7; LOC105376737; LOC105376806; LOC107984915; CELA2B; MIR7846; MIR429; LOC105378612; DDI2; MIB2; FNDC10; LINC01134; DISP3; RERE-AS1; TMEM88B; CFAP74; RNU6-828P; KLHL21; CLCNKA; SZRD1; SLC2A7; PGD; CDK11A; SKI; FAAP20; LOC105376740; LOC107985728; PRXL2B; SLC35E2A; HES2; TP73; NOL9; SRM; CELA2A; LOC102724429; LOC100288379; SPEN; LOC105376717; AGTRAP; PRAMEF25; MTOR; RPL7AP18; RN7SL649P; NADK; TNFRSF25; See more...

Location information:

Clinical significance:

ID:: 53636067

variant

5.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: LOC107985467; LINC01777; LOC105376674; PADI1; CPLANE2; KLHL21; RNU6-1099P; LOC105376717; SLC25A33; LOC100129776; SPSB1; AKR7L; EPHA2-AS1; RNF207; GPR153; MIR6730; EFHD2; IFFO2; PDPN; CAMTA1-AS2; LOC105376817; LOC107985736; SPEN; DDI2; PRDM2; IGSF21-AS1; RNU6-777P; HTR6; C1orf167; VPS13D; MIR1290; TRG-CCC1-1; KLHDC7A; DFFA; LOC105376737; RNU6ATAC18P; TRG-CCC4-1; HSPB7; NMNAT1; RNU1-6P; PLA2G2A; PRAMEF17; SPEN-AS1; HMGN2P17; UBXN10; EIF1AXP1; LOC105376691; PGAM1P11; MIR5697; PLA2G2D; LOC107985469; RBP7; CAMTA1; PRAMEF14; TRG-CCC5-1; RNU7-179P; ZBTB17; LINC01647; SLC25A34; RPL39P6; RNU6-291P; HNRNPCL4; RN7SL451P; CASP9; FAM131C; KIF1B; DHRS3; CTRC; RPL23AP19; AADACL3; CAMTA1-DT; RPL37P9; TRE-TTC4-1; PIK3CD-AS1; CLSTN1; TRV-CAC13-1; MIR34AHG; PDE4DIPP8; ZBTB2P1; FBXO2; PRAMEF18; CA6; RERE; PHF13; LOC105376733; LOC105376756; ACTL8; PLA2G5; RNU4-28P; RNU6-37P; ARHGEF10L; DNAJC16; MFFP1; ICMT-DT; MIR4695; MFAP2; DYNLL1P3; LOC105376739; RNU6-731P; SDHB; CASZ1; LOC105376759; KAZN-AS1; NECAP2; PLOD1; PRAMEF6; MICOS10-DT; PRAMEF15; LOC105376825; KIAA2013; LOC105376805; LINC01646; LINC01672; ESPNP; CROCC; EFHD2-AS1; FBLIM1; AADACL4; PER3; LNCTAM34A; MIR6729; RNU1-7P; RNU6-1072P; HES3; LINC01654; TBCAP2; PLEKHM2; MIR6728; PRAMEF27; MIR4632; LOC105376819; AKR7A2; RPL21P21; ZBTB48; RNA5SP41; EXOSC10-AS1; CTNNBIP1; NBL1; UBE4B; TRV-CAC11-1; LOC107984911; KCNAB2; VAMP3; ANO7L1; FHAD1; PRAMEF11; CFAP107; PLA2G2E; ARHGEF19; PRAMEF31P; FHAD1-AS1; CORT; MIR4252; LOC105376695; TNFRSF1B; SLC66A1; NPHP4; PRAMEF19; MICOS10-NBL1; CENPS-CORT; RNU6-771P; CLCN6; MFN2; ENO1-AS1; HNRNPCL3; TMEM51-AS2; FBXO42; PADI6; RPL22P3; PRAMEF36P; RNA5SP40; PRAMEF35P; LINC02783; IGSF21; ESPN; ERRFI1; PARK7; RNU6-537P; LINC01783; TMEM51-AS1; EMC1-AS1; RN7SL277P; RPL7P7; PRAMEF7; TMEM82; HSPE1P24; SLC45A1; LOC105376735; LOC112268261; MIR3972; SRARP; LOC107984913; SLC2A5; LRRC38; LOC105376818; TNFRSF9; LOC101060126; PLA2G2F; CENPS; CROCCP2; PRAMEF29P; MTCYBP45; LOC105376712; MZT1P1; PRAMEF28P; TARDBP; MIR7846; LINC02782; NPPA; UBR4; PRAMEF4; UBE2V2P3; CELA2B; HNRNPCL2; PRAMEF5; LINC02766; SBF1P2; PAX7; OTUD3; DNAJC11; LINC01714; PRAMEF10; AGMAT; PIK3CD; RNU1-2; MTOR-AS1; NBPF1; PRAMEF1; RNU1-4; C1orf167-AS1; RNU5E-4P; LOC105376767; RPL22; RN7SKP269; RNU6-1265P; CROCCP3; LOC105376806; ALDH4A1; LOC105376740; MTOR; CHCHD2P6; MT1XP1; RNF207-AS1; MRTO4; CLCNKB; LZIC; RPS16P1; LOC105378612; LOC105376823; AKR7A3; PADI3; RERE-AS1; RPL7AP18; PGD; FBXO44; TMEM201; RN7SL649P; SRM; RPS14P3; MIR34A; RCC2; RPL9P11; CLCNKA; RSC1A1; ANGPTL7; PADI2; PLA2G2C; SLC2A7; LOC107984918; DRAXIN; SZRD1; TRG-CCC1-2; SNORA59A; PRAMEF25; CELA2A; MIR3675; LOC107984915; PRAMEF30P; BRWD1P1; RNU1-3; TNFRSF25; CD24P1; LOC102724429; PRAMEF26; PRAMEF20; SCARNA21B; HES2; AGTRAP; NOL9; RNU5E-1; LINC02781; LOC107984912; DISP3; SLC25A34-AS1; ENO1; TRUND-NNN4-1; RNF186; RNU6-828P; TMEM274P; RNU1-8P; PLEKHG5; PRAMEF33; H6PD; PRAMEF34P; LOC101056699; RNU1-5P; PIK3CD-AS2; GPR157; LOC107985101; PRAMEF9; CAPZB; CAMTA1-AS1; CFL1P6; TRV-CAC11-2; PRAMEF12; SPATA21; MAD2L2; ATP13A2; UTS2; MST1P2; FAM131C2P; TRN-GTT5-1; PRAMEF8; MIIP; LOC105376686; NPPA-AS1; PADI4; LOC102724856; ICMT; RPL23AP89; LOC105376689; EMC1; AJAP1; KAZN; ACOT7; TRE-TTC3-1; TAS1R1; RNU6-991P; LOC105376809; MST1L; LINC02810; LINC01772; MICOS10; LOC100506730; EPHA2; LOC112267871; NPPB; LOC105376815; RNU6-304P; TRN-GTT4-1; TNFRSF8; LOC105376812; THAP3; PRAMEF13; RPL7P11; PEX14; RN7SL304P; TAS1R2; LINC01784; PDE4DIPP9; LOC105376682; TMCO4; C1orf127; CHD5; FBXO6; RN7SL614P; LOC105376808; MTHFR; TRN-GTT13-1; RPL12P14; RN7SL731P; MASP2; RPL26P7; SNORD128; PRAMEF32P; RPL27P3; PRAMEF2; CROCCP4; LOC100419911; TMEM51; EXOSC10; UQCRHL; HNRNPCL1; LINC02606; RPL10P17; RNU1-1; UBIAD1; MIR4689; See more...

Location information:

Clinical significance:

ID:: 55279460

variant

6.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: MFFP1; RPL21P21; PRAMEF27; TRV-CAC11-1; PRAMEF18; MIR4632; MIR6728; CA6; ICMT-DT; LINC02780; LOC105376756; RNU6-731P; FBXO2; CLSTN1; LRRC47; PIK3CD-AS1; EXOSC10-AS1; LOC105376759; MFAP2; LINC01646; LOC105378608; SLC25A34; LOC105376739; ZBTB17; RERE; EIF1AXP1; LNCTAM34A; PADI3; CTRC; CASP9; LOC107984911; SPEN-AS1; NPPA; KAZN-AS1; RNU1-7P; DNAJC16; PRAMEF14; WRAP73; CAMTA1-DT; MIR6729; FAM131C; LINC01672; LOC105376805; RNA5SP41; EFHD2-AS1; DHRS3; RNU6-1072P; RBP7; AADACL3; ARHGEF10L; TRG-CCC5-1; CAMTA1; PRAMEF10; RNU1-2; CROCCP3; LINC01783; CHCHD2P6; LOC105376695; TP73-AS3; TRUND-NNN4-1; PRAMEF35P; TPRG1L; RPL22; PRAMEF1; FBXO44; HSPE1P24; PRAMEF29P; LOC105376712; MIR4252; LINC01345; LOC105376735; MZT1P1; CROCCP2; TARDBP; LOC100420339; HNRNPCL2; SLC2A5; TNFRSF9; GFOD3P; ANO7L1; RNU6-771P; LOC107984913; RNU6-537P; PRDM16; NBPF1; SBF1P2; DNAJC11; FHAD1-AS1; RNU1-4; PRAMEF5; LZIC; AGMAT; PRAMEF4; CELA2B; RNA5SP40; PRAMEF31P; PIK3CD; CLCNKB; MT1XP1; CENPS-CORT; ESPN; RN7SKP269; PRAMEF7; CENPS; PADI6; LINC01714; LINC02783; TMEM51-AS1; ERRFI1; LRRC38; TNFRSF1B; MIR3972; RNU6-1265P; PRAMEF11; RPL7P7; SRARP; CORT; LINC02766; PRAMEF19; UBE2V2P3; MTCYBP45; LINC02782; CFAP107; MTOR-AS1; ARHGEF19; LOC112268261; FHAD1; PRAMEF28P; MFN2; LOC101060126; FBXO42; ENO1-AS1; RNU5E-4P; C1orf167-AS1; SLC45A1; RNF207-AS1; LOC105376767; TMEM51-AS2; RPL22P3; PRAMEF36P; NPHP4; CLCN6; HNRNPCL3; TMEM82; MIR7846; PARK7; PRAMEF9; TRE-TTC3-1; PRAMEF8; LOC107985101; ATP13A2; BRWD1P1; MST1P2; MIIP; ICMT; MIR3675; CAMTA1-AS1; KAZN; TRG-CCC1-2; LOC107984915; LOC107984912; PEX14; PRAMEF34P; GPR157; LOC105376717; MST1L; CCDC27; H6PD; LOC105378612; LOC105376806; LINC02781; LOC105376740; RNU6-828P; SPATA21; LOC102724429; MAD2L2; LOC107984918; EPHA2; UTS2; PADI4; PLEKHG5; PRAMEF26; DFFB; ACOT7; AJAP1; NPPA-AS1; PRAMEF12; TAS1R1; SCARNA21B; RNU6-304P; PRAMEF33; CFL1P6; RN7SL649P; SRM; LINC01134; FAM131C2P; RNU1-3; RERE-AS1; LOC102724856; TRN-GTT5-1; RNU5E-1; CD24P1; CELA2A; DRAXIN; PADI2; RPL9P11; MTOR; PRAMEF20; RN7SL614P; RNU6-991P; PIK3CD-AS2; PRAMEF30P; EEF1DP6; SNORA59A; SLC25A34-AS1; ANGPTL7; ENO1; LOC105378604; LOC105376689; AGTRAP; PRAMEF25; SLC2A7; TMEM274P; RNU1-8P; RPS16P1; LINC01772; RNU1-5P; LOC101056699; TP73; DISP3; TRV-CAC11-2; LOC105376686; HES2; NOL9; RPL7AP18; TNFRSF25; LOC112267871; PRAMEF17; NMNAT1; MIR4251; RN7SL731P; TRN-GTT13-1; RCC2; RSC1A1; CLCNKA; RPL23AP89; TRG-CCC1-1; MIR34A; PGD; TMEM201; HSPB7; SZRD1; RPL27P3; KLHL21; LINC02606; MIR4689; SMIM1; C1orf167; RPL26P7; SPEN; GPR153; PRDM2; LINC01777; VPS13D; LINC01784; LINC01346; SNORD128; CPLANE2; PADI1; SLC25A33; PRDM16-DT; RNF207; CROCCP4; HNRNPCL1; SPSB1; RN7SL574P; EFHD2; ACTRT2; RPL7P11; ZBTB48; PDPN; DDI2; CEP104; LOC107984909; PDE4DIPP9; LOC105376808; PRAMEF2; LOC105376674; DFFA; RNU6-777P; LOC105378606; C1orf127; UBIAD1; RNU1-1; RNU6ATAC18P; MIR6730; MIR5697; LOC105376691; LOC105376682; TMEM51; LOC100129776; TRN-GTT4-1; LOC107985467; MASP2; RNU1-6P; CAMTA1-AS2; CHD5; C1orf174; TRG-CCC4-1; AADACL4; LOC107985736; RPL10P17; RPL12P14; MTHFR; EXOSC10; EPHA2-AS1; UQCRHL; NPPB; PRAMEF32P; FBXO6; LOC105376737; TRE-TTC4-1; PDE4DIPP8; TNFRSF8; ZBTB2P1; LOC105378605; PRAMEF13; VAMP3; LINC01647; RNU6-37P; KIAA2013; LOC105376733; KCNAB2; RNU7-179P; PGAM1P11; PLOD1; SDHB; CTNNBIP1; PRAMEF15; PLEKHM2; ARHGEF16; THAP3; PER3; RPL39P6; FBLIM1; LOC107985469; PRAMEF6; HMGN2P17; NECAP2; HES3; TBCAP2; MIR551A; CASZ1; RPL37P9; ESPNP; HNRNPCL4; TRV-CAC13-1; MEGF6; RN7SL451P; RNU6-291P; UBE4B; PHF13; KIF1B; CROCC; RPL23AP19; MIR34AHG; See more...

Location information:

Clinical significance:

ID:: 48463856

variant

7.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: RN7SL451P; RNU6-291P; PRAMEF18; HNRNPCL4; C1orf159; DHRS3; RPL23AP19; FBXO2; MORN1; MIR34AHG; ATAD3C; ANKRD65-AS1; LOC105376733; CCNL2; PIK3CD-AS1; RPL37P9; AADACL3; PRAMEF14; LINC01647; MRPL20-AS1; ICMT-DT; RERE; NPPA; TMEM240; TAS1R3; LOC105378605; CAMTA1; LOC105378602; RNU6-37P; PRAMEF10; RN7SL657P; MIR200B; TMEM52; LOC284600; RPL39P6; RBP7; LRRC47; WRAP73; PGAM1P11; MTOR-AS1; HMGN2P17; CFL1P6; CLSTN1; CPTP; TNFRSF4; ACOT7; PUSL1; LOC105376686; LOC105378598; PRAMEF9; DFFB; MIIP; UTS2; ATAD3B; RPL23AP89; LOC105378601; PRKCZ; AJAP1; ICMT; PRAMEF12; RNU6-304P; KAZN; PEX10; LOC107984904; LOC105378604; TNFRSF14-AS1; INTS11; LOC105376689; PEX14; LOC102724856; CDK11B; RNU6-991P; PRAMEF8; LINC01770; MIR200A; PLEKHG5; MIR6808; HES4; TMEM274P; H6PD; PRAMEF34P; PIK3CD-AS2; PRKCZ-AS1; FAM41C; CCDC27; TAS1R1; MAD2L2; RNU1-8P; GPR157; MMEL1; RNA5SP40; SLC45A1; PARK7; CENPS-CORT; MIR6727; B3GALT6; GNB1; NPHP4; PRAMEF36P; RNU6-537P; CLCN6; RNF223; PRAMEF31P; PRAMEF7; ERRFI1; CENPS; HNRNPCL3; MMP23B; LRRC38; LOC105376735; LOC105376712; NPPA-AS1; ESPN; PRAMEF35P; MZT1P1; CORT; RN7SL614P; HSPE1P24; LOC107984850; LOC107984913; TNFRSF1B; LOC105376695; TRUND-NNN4-1; MIR4252; TP73-AS3; RPL7P7; PRAMEF19; LINC01345; LOC105378590; RNU6-771P; CFAP107; LINC01128; SAMD11; PRAMEF11; GPR153; PLCH2; LINC02593; RNF207; RPL39P12; RNU6ATAC18P; MIR6726; PDPN; CAMTA1-AS2; DFFA; C1orf167; SPSB1; PLEKHN1; LOC100129381; CALML6; TTLL10; PRAMEF17; VPS13D; SCNN1D; LOC105376691; LOC105378606; MIR5697; RNU6-777P; LOC107984909; LINC01346; MIR6730; LOC105378589; AGRN; AURKAIP1; LOC105376674; LOC105378586; LOC105376737; SLC25A33; LOC107985467; PRDM16-DT; KLHL21; CEP104; SMIM1; PRDM2; LINC01777; UBE2J2; CDK11A; PGD; MIR34A; PRXL2B; LOC100129776; TMEM201; SNORA59A; DISP3; CFAP74; RNU6-828P; HES2; LINC01134; TTC34; ENO1; PRAMEF33; NMNAT1; LINC01342; TNFRSF14; TNFRSF18; RN7SL649P; EEF1DP6; PRAMEF26; RNU5E-1; CAMTA1-AS1; LOC107984872; TNFRSF25; NADK; LOC102724429; PRAMEF30P; DRAXIN; ATAD3A; BRWD1P1; PRAMEF20; SRM; RERE-AS1; LOC107984918; RPL9P11; ANGPTL7; LOC105378612; LINC02781; AGTRAP; LOC107984915; NOL9; FAM87B; LOC107984912; PRAMEF25; TP73; SKI; FNDC10; MIR429; LOC105376717; LOC100288379; SNORD167; TMEM88B; MIB2; LOC107985728; SLC35E2A; TBCAP2; MIR551A; MTOR; LOC105376740; FAAP20; MEGF6; LOC112268220; MMP23A; MIR6728; ANKRD65; UBE4B; MIR4632; SLC2A7; RNU1-7P; RNU6-1072P; PERM1; RPL7AP18; ARHGEF16; RNA5SP41; LOC107984911; KCNAB2; LOC105378608; VAMP3; ISG15; LOC100996583; LINC01786; CA6; LINC01672; SDF4; PHF13; PRAMEF27; CTNNBIP1; PANK4; RNU6-731P; LINC02780; LOC105376756; CAMTA1-DT; KIF1B; KIAA2013; PRAMEF6; LINC01646; RPL21P21; HES3; LNCTAM34A; RN7SL574P; RPL10P17; PRKCZ-DT; LOC105376739; RN7SL731P; SSU72; PRAMEF15; NOC2L; EXOSC10-AS1; FBXO6; THAP3; LINC02606; KLHL17; AADACL4; C1orf174; MTHFR; MRPL20; RER1; LOC105376682; C1orf127; PLOD1; KAZN-AS1; UBIAD1; PRAMEF2; LOC100288175; PER3; SLC35E2B; TUBB8P11; CASZ1; MIR4689; CHD5; MIR4251; GNB1-DT; MASP2; NPPB; HNRNPCL1; HES5; ZBTB48; TNFRSF8; ACTRT2; PRAMEF32P; LOC105378600; SNORD128; GABRD; VWA1; EXOSC10; MMEL1-AS1; MIR6729; LINC01784; PRAMEF13; LOC112268219; MXRA8; RPL7P11; PRAMEF5; ACAP3; C1orf167-AS1; RNF207-AS1; DNAJC11; LOC105378599; RPL27P3; RPL26P7; RPL22; TPRG1L; LZIC; LOC100129534; SBF1P2; LINC01714; RN7SKP269; GFOD3P; SLC2A5; PRAMEF29P; PRDM16; UBE2V2P3; PRAMEF28P; LINC00115; LOC112268261; HNRNPCL2; MFN2; FBXO44; LOC105378948; LOC105378593; LOC101060126; MIR7846; TNFRSF9; LINC02782; MTCYBP45; LOC100420339; ENO1-AS1; C1QTNF12; TARDBP; LINC02766; PIK3CD; TTLL10-AS1; LOC107985732; LOC112268218; RNU5E-4P; NDUFB4P8; PRAMEF1; RNU6-1265P; DVL1; LOC107985729; PRAMEF4; See more...

Location information:

Clinical significance:

ID:: 48436385

variant

8.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: PDPN; PADI1; CPLANE2; RN7SL649P; KLHL21; LOC107984918; LOC105376806; SPSB1; PRDM2; LOC100129776; RERE-AS1; RNU6-828P; VPS13D; GPR153; SPEN; SCARNA21B; DDI2; PRAMEF30P; RNF207; HES2; C1orf167; EFHD2; TNFRSF25; BRWD1P1; LOC107985101; SLC25A33; PRAMEF17; NMNAT1; HSPB7; LOC107984915; LOC105376740; LOC107984912; TRG-CCC1-1; LNCTAM34A; EFHD2-AS1; PDE4DIPP9; KAZN-AS1; MIR6729; LOC105378612; MTHFR; TMEM51; RNU6-1072P; LOC105376805; TRN-GTT4-1; CROCCP4; LINC02606; RNU1-7P; PRAMEF13; EXOSC10; HNRNPCL1; RPL27P3; RPL10P17; UQCRHL; CHD5; RNA5SP41; RPL12P14; MIR6728; THAP3; UBIAD1; DFFA; FBXO6; PRAMEF27; MIR4689; PRAMEF2; LOC107984911; TRN-GTT13-1; PRAMEF32P; LOC105376759; NPPB; RPL7P11; MASP2; RNU1-1; C1orf127; TNFRSF8; LOC105376739; RNU6-731P; EXOSC10-AS1; RPL26P7; HES3; PER3; CASZ1; LINC01784; PLOD1; SNORD128; FBLIM1; LOC105376808; NECAP2; PRAMEF6; ESPNP; CROCC; TBCAP2; PLEKHM2; ZBTB48; MIR4632; RN7SL731P; AADACL4; VAMP3; UBE4B; LOC107985736; RPL21P21; CTNNBIP1; SDHB; KCNAB2; TRV-CAC11-1; KIAA2013; PRAMEF15; RPL37P9; LOC101060126; CLSTN1; PRAMEF28P; KIF1B; LOC112268261; LOC105376767; CASP9; FAM131C; MTOR-AS1; TRG-CCC5-1; MTCYBP45; HMGN2P17; LINC02766; EIF1AXP1; PGAM1P11; RPL39P6; RBP7; C1orf167-AS1; RNU5E-4P; LINC01672; CTRC; AADACL3; DHRS3; ARHGEF10L; RNF207-AS1; TRV-CAC13-1; RN7SL451P; FBXO2; MIR7846; RPL23AP19; ZBTB2P1; ACTL8; CA6; MFAP2; PDE4DIPP8; ICMT-DT; PIK3CD-AS1; LINC01714; PRAMEF18; DNAJC16; RN7SKP269; PRAMEF14; CAMTA1-DT; RNU6-37P; SPEN-AS1; CAMTA1; RERE; ZBTB17; MFFP1; SLC25A34; UBE2V2P3; CROCCP2; RNU6-1265P; PHF13; PRAMEF4; RPL22; AGMAT; HNRNPCL2; CLCNKB; PRAMEF5; DNAJC11; HNRNPCL4; LZIC; MT1XP1; MIR34AHG; RNU1-4; TARDBP; PRAMEF10; SBF1P2; CELA2B; SLC2A5; PIK3CD; LINC01654; CROCCP3; NBPF1; RNU6-291P; TNFRSF9; PRAMEF29P; LOC105376756; PRAMEF1; LOC105376733; PADI3; FBXO44; RNU1-2; NPPA; PRAMEF19; FHAD1; LOC105376809; TRE-TTC4-1; LINC02810; LINC01772; TMEM82; LOC105376812; SLC45A1; RNU7-179P; LOC107985469; TRN-GTT5-1; PRAMEF31P; PRAMEF36P; CLCN6; PADI6; RPL22P3; LINC01647; IGSF21; PRAMEF11; FBXO42; ENO1-AS1; LINC01783; TMEM274P; HNRNPCL3; ERRFI1; CFAP107; PRAMEF35P; RN7SL614P; LRRC38; MFN2; RPL23AP89; LOC105376686; CENPS; SRARP; LOC112267871; CHCHD2P6; LOC102724856; TNFRSF1B; LOC105376689; CENPS-CORT; NPHP4; ESPN; RNU1-8P; RNU6-304P; PRAMEF7; LOC105376712; PARK7; LOC101056699; TMEM51-AS2; PIK3CD-AS2; RNU1-5P; TAS1R1; SLC25A34-AS1; TMEM51-AS1; EPHA2; RNU6-771P; RNU6-991P; ACOT7; RNA5SP40; RNU6-537P; GPR157; H6PD; MAD2L2; TRUND-NNN4-1; RPL7P7; ATP13A2; MIR4252; ARHGEF19; PRAMEF12; FAM131C2P; LOC105376735; MIR3972; LINC02783; UTS2; ICMT; PADI4; SPATA21; TRE-TTC3-1; MZT1P1; PEX14; KAZN; ANO7L1; PRAMEF8; MST1P2; HSPE1P24; MIIP; TRV-CAC11-2; PRAMEF34P; DISP3; MST1L; NOL9; RNU6ATAC18P; NPPA-AS1; CFL1P6; RCC2; PRAMEF9; SNORA59A; LOC107984913; RSC1A1; PLEKHG5; TMEM201; CAMTA1-AS2; CORT; TRG-CCC4-1; LOC105376695; ENO1; PRAMEF20; LOC105376691; PRAMEF33; MIR5697; RNU5E-1; FHAD1-AS1; RNU1-6P; CAMTA1-AS1; CELA2A; MIR6730; MIR3675; CD24P1; EPHA2-AS1; RNU6-777P; LOC107985467; AGTRAP; DRAXIN; PRAMEF26; RNU1-3; TRG-CCC1-2; LOC105376737; RPL7AP18; PGD; PADI2; ANGPTL7; RPL9P11; SLC2A7; CLCNKA; MIR34A; IGSF21-AS1; SZRD1; SRM; MTOR; LOC105376717; RPS16P1; PRAMEF25; See more...

Location information:

Clinical significance:

ID:: 48463591

variant

9.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: AURKAIP1; LOC105376691; PRDM16-DT; MIR6859-2; RNU6-1100P; CALML6; UBE2J2; MIR5697; LINC01346; UBIAD1; LOC105378606; SLC25A33; CEP104; MTCO3P12; WBP1LP7; LOC100129776; MIR6730; MTATP6P1; LOC105378586; TTLL10; NPPB; LINC01777; RNF207; CAMTA1-AS2; DFFA; PLCH2; LINC02593; HES5; MIR6726; AGRN; SMIM1; VWA1; RPL39P12; PLEKHN1; GPR153; LOC100129381; SPSB1; SCNN1D; LINC01409; KLHL17; HSPE1P24; RNU6ATAC18P; CENPS; OR4F29; LINC01345; TRUND-NNN4-1; PEX14; RPL7P7; LOC105376695; TP73-AS3; RN7SL614P; TNFRSF1B; MIR4252; MZT1P1; SAMD11; LOC105376735; LOC105378590; CORT; ATAD3B; LOC107984904; PLEKHG5; SEPTIN14P13; MAD2L2; CCDC27; DFFB; LINC01128; PRKCZ; LOC105378604; LOC105376689; RNA5SP40; TMEM274P; GNB1; RNU6-537P; LOC105376712; ESPN; RNU6-304P; ERRFI1; B3GALT6; CENPS-CORT; SLC45A1; MIR6727; INTS11; RNF223; NPPA-AS1; FAM41C; PARK7; MIR200A; PIK3CD-AS2; RNU5E-1; MIR6808; OR4F16; CDK11B; RNU6-991P; LOC100132287; MMEL1; PERM1; GPR157; RNU1-8P; PRKCZ-AS1; SKI; H6PD; CPTP; AJAP1; LINC01770; CFL1P6; RPL23AP89; LOC112268220; CFAP74; PUSL1; TNFRSF14-AS1; TAS1R1; LOC105378598; ACOT7; TMEM201; TNFRSF4; HES4; MIR34A; ENO1; ICMT; UTS2; LOC102723897; LOC105376686; LOC105378601; RPL9P11; MIIP; PEX10; RNU6-37P; LINC01647; MRPL20-AS1; ANKRD65-AS1; NPPA; LRRC47; RN7SL657P; PGAM1P11; LOC729737; MTCYBP45; WBP1LP6; RBP7; MIR200B; LOC101060126; NDUFB4P8; MTATP8P1; HMGN2P17; PIK3CD; ACAP3; DHRS3; RPL37P9; LOC107985732; RN7SL451P; LOC105378599; CCNL2; MTOR-AS1; LINC01714; LOC105378602; MIR34AHG; SBF1P2; LOC105378605; PIK3CD-AS1; ATAD3C; CLSTN1; RPL23AP19; C1orf159; DVL1; LOC105376733; PRDM16; FBXO2; RPL22; TMEM240; LOC107984913; UBE2V2P3; FBXO44; TARDBP; LOC100420339; LOC100129534; LOC105378948; TTLL10-AS1; LOC105378593; LOC112268261; C1QTNF12; LOC107984850; GFOD3P; MTND2P28; GTF2IP10; LINC02782; ENO1-AS1; LOC107985729; RNU5E-4P; DNAJC11; SLC2A5; LINC00115; C1orf167-AS1; LINC02766; LOC112268218; RNF207-AS1; MXRA8; NPHP4; MTND1P23; TNFRSF9; LZIC; CLCN6; MIR7846; WASH9P; TPRG1L; MFN2; MIR4689; RNU6-731P; RPL23AP21; RN7SKP269; TUBB8P11; GNB1-DT; RPL26P7; MMP23B; RPL27P3; MIR6729; HES3; MTCO2P12; RPL23AP24; PLOD1; MTCO1P12; LOC112268219; KCNAB2; C1orf174; RER1; SNORD128; TNFRSF8; LINC01646; CICP27; MASP2; LOC100288069; LOC100288175; EXOSC10; RNU1-7P; LOC105378600; ZBTB48; ACTRT2; MIR4251; GABRD; RPL10P17; MTHFR; RPL7P11; MRPL20; LOC105376682; MMEL1-AS1; LINC02606; DDX11L17; SDF4; KIAA2013; CTNNBIP1; THAP3; SSU72; FBXO6; EXOSC10-AS1; CICP7; SEPTIN14P14; RN7SL574P; PHF13; LOC105376739; RERE; LOC105378608; CASZ1; CHD5; C1orf127; LNCTAM34A; RNU6-1199P; CAMTA1; SNORD167; RN7SL731P; PER3; LOC284600; WRAP73; NOC2L; LINC01672; SLC35E2B; MIR4632; LOC101928626; ICMT-DT; ARHGEF16; LOC100996583; LINC02780; MIR551A; CA6; RNU6-291P; MEGF6; LINC01786; LOC107984911; VAMP3; ANKRD65; CAMTA1-DT; UBE4B; PRKCZ-DT; RPL21P21; SEPTIN14P18; MORN1; TAS1R3; MIR6728; MMP23A; FAM87B; LOC105376674; KIF1B; ISG15; LOC105378589; DRAXIN; AGTRAP; LOC107984912; MTOR; ANGPTL7; LOC107984915; RPL39P6; LOC105376717; SLC2A7; CAMTA1-AS1; LOC105378947; FNDC10; FAAP20; LINC02781; MIB2; TMEM52; PANK4; KLHL21; NADK; LOC107985728; PRXL2B; C1orf167; RNU6-828P; CICP3; LOC105376740; RPL7AP18; HES2; PGD; CDK11A; MIR12136; TNFRSF25; DISP3; RN7SL649P; NOL9; LOC102724429; SLC35E2A; LINC01342; TTC34; LOC107984872; LINC01134; SRM; LOC105376737; NMNAT1; LOC107984909; VPS13D; ATAD3A; TMEM88B; TNFRSF18; LOC112268260; MIR429; RERE-AS1; TP73; LOC100288379; TNFRSF14; EEF1DP6; SNORA59A; RNU6-777P; See more...

Location information:

Clinical significance:

ID:: 48451788

variant

10.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: GPR157; MST1L; RPL7AP18; LOC105376806; LOC107984918; RNU1-8P; LOC107984915; PIK3CD-AS2; ATP13A2; RCC2; BRWD1P1; MIR34A; RPL9P11; LOC112267871; MIIP; RPS16P1; PRAMEF20; ENO1; RPL23AP89; PRAMEF33; SZRD1; PGD; PADI2; UTS2; RSC1A1; PRAMEF12; RNU1-3; RNU5E-1; PRAMEF9; LINC01772; CFL1P6; LOC105376809; RN7SL649P; KAZN; TMEM201; SCARNA21B; FAM131C2P; LOC105376740; PADI1; MTOR; DDI2; PRAMEF25; LOC105378612; LOC100129776; TRG-CCC1-2; DRAXIN; LOC105376737; SLC2A7; LOC105376717; PRDM2; EPHA2-AS1; MIR5697; AGTRAP; TRG-CCC1-1; CAMTA1-AS1; CELA2A; SRM; RNU6ATAC18P; LOC107985101; PRAMEF30P; VPS13D; RERE-AS1; CAMTA1-AS2; ANGPTL7; NMNAT1; SNORA59A; CLCNKA; PRAMEF26; MIR3675; MIR1290; EFHD2; RNU6-777P; CD24P1; RNU6-828P; DISP3; SPEN; PDPN; C1orf167; CPLANE2; RPL7P11; MIR6730; HSPB7; SLC25A33; NPPB; MASP2; LOC107985467; RNU1-6P; PRAMEF17; PRAMEF32P; TRN-GTT13-1; IGSF21-AS1; TRG-CCC4-1; UBIAD1; LOC107985736; IFFO2; LOC105376691; RPL10P17; KLHDC7A; MTHFR; SPSB1; DFFA; TRN-GTT4-1; LOC105376805; LOC105376808; SNORD128; TMEM51; MIR6729; KAZN-AS1; DYNLL1P3; SDHB; PRAMEF13; PDE4DIPP9; EXOSC10; PRAMEF6; PLOD1; TAS1R2; RPL27P3; TRV-CAC11-1; PRAMEF15; RPL26P7; RN7SL731P; TNFRSF8; LINC02606; MIR4632; PRAMEF2; PRAMEF27; RNU1-1; HNRNPCL1; C1orf127; LINC01784; UQCRHL; RPL12P14; RPL21P21; RNU6-1072P; RNU1-7P; AADACL4; CROCCP4; FBXO6; RPL39P6; CAMTA1; SLC25A34; TRG-CCC5-1; FAM131C; PLEKHM2; EFHD2-AS1; SPEN-AS1; LINC01672; FBLIM1; CAMTA1-DT; KIAA2013; KIF1B; CASZ1; RERE; DNAJC16; LNCTAM34A; MFAP2; NECAP2; PER3; VAMP3; PDE4DIPP8; EXOSC10-AS1; ZBTB2P1; LOC107985469; PIK3CD-AS1; CTNNBIP1; CA6; LOC105376756; LOC105376739; LINC01654; MIR6728; LOC105376759; HNRNPCL4; MFFP1; ESPNP; RNA5SP41; RNU7-179P; LOC105376733; MIR4695; UBE4B; TRE-TTC4-1; TRV-CAC13-1; CROCC; RPL37P9; PGAM1P11; PRAMEF4; CASP9; RBP7; HMGN2P17; TBCAP2; CTRC; EIF1AXP1; PRAMEF18; ZBTB17; PRAMEF14; RNU6-37P; FBXO44; RNU6-291P; PADI3; CROCCP2; LOC101060126; NPPA; FBXO2; RNU5E-4P; PRAMEF29P; RN7SKP269; MTOR-AS1; MTCYBP45; AADACL3; CROCCP3; LOC105376767; PRAMEF5; LINC01647; PRAMEF10; MIR34AHG; ACTL8; AGMAT; CFAP107; ARHGEF10L; RN7SL451P; PRAMEF1; LINC01714; LOC112268261; CLSTN1; PRAMEF11; UBE2V2P3; LINC02766; SLC2A5; SRARP; RPL23AP19; PIK3CD; TNFRSF9; PRAMEF28P; DHRS3; SBF1P2; TMEM82; ALDH4A1; CHCHD2P6; MIR3972; PRAMEF7; TMEM51-AS1; SLC45A1; TARDBP; MT1XP1; PRAMEF35P; C1orf167-AS1; DNAJC11; RNU6-537P; PADI6; CLCN6; LZIC; ENO1-AS1; RPL22P3; LRRC38; HNRNPCL3; ANO7L1; RNA5SP40; RNU1-4; HNRNPCL2; CLCNKB; RNU6-1265P; LOC105376695; EPHA2; TMEM274P; PRAMEF34P; PRAMEF19; LOC101056699; H6PD; RNU1-2; RNU1-5P; CENPS; FHAD1; TNFRSF1B; RN7SL614P; CELA2B; PAX7; HSPE1P24; PEX14; LOC105376735; MIR7846; MZT1P1; NBPF1; MFN2; RNU6-991P; TMEM51-AS2; SLC25A34-AS1; RNU6-304P; LINC01783; LOC105376712; LOC102724856; TRN-GTT5-1; LOC105376689; LINC02783; TRV-CAC11-2; SPATA21; ERRFI1; TRE-TTC3-1; LOC105376812; LINC02810; PRAMEF8; FBXO42; FHAD1-AS1; PADI4; MAD2L2; RNU6-771P; PRAMEF31P; ARHGEF19; PRAMEF36P; TRUND-NNN4-1; RPL7P7; CORT; NPPA-AS1; PARK7; MST1P2; CENPS-CORT; IGSF21; See more...

Location information:

Clinical significance:

ID:: 54355614

variant

11.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: PARK7; RNF223; SLC45A1; ERRFI1; LINC01345; MIR6727; MMP23B; TRUND-NNN4-1; B3GALT6; CORT; LOC105376695; MIR4252; RPL7P7; TP73-AS3; MZT1P1; ESPN; PEX14; LOC105376735; LOC105376712; CENPS; RN7SL614P; HSPE1P24; OR4F29; LINC01128; NPHP4; LOC105378590; SAMD11; PRKCZ; RNU6-537P; CENPS-CORT; RNA5SP40; GNB1; GTF2IP10; RPL21P21; LINC01786; ISG15; UBE4B; PHF13; MIR6728; MMP23A; ANKRD65; RERE; LOC107984911; PANK4; ARHGEF16; LOC105378608; EXOSC10-AS1; ICMT-DT; CA6; VAMP3; LOC101928626; CTNNBIP1; LINC01646; CICP7; NOC2L; SDF4; LOC105376739; CICP27; CAMTA1; CASZ1; LNCTAM34A; LINC02780; LOC100996583; CAMTA1-DT; SEPTIN14P18; LINC01672; SLC35E2B; PER3; SNORD167; MIR551A; KIF1B; MEGF6; PRKCZ-DT; SEPTIN14P14; C1orf159; LINC01714; LOC105378605; MORN1; TAS1R3; PIK3CD-AS1; CCNL2; LOC105378602; FBXO2; MRPL20-AS1; ATAD3C; RNU6-1199P; TMEM240; ANKRD65-AS1; LOC729737; MIR200B; LOC105376733; TMEM52; RNU6-37P; RN7SL657P; LRRC47; WBP1LP6; PGAM1P11; MTATP8P1; HMGN2P17; WRAP73; LINC01647; RPL39P6; LOC107985732; LOC284600; MIR34AHG; RBP7; RN7SL451P; MTOR-AS1; RPL37P9; RPL23AP19; RNU6-291P; LOC100129381; CLSTN1; AGRN; MIR6726; LOC107984909; SCNN1D; CALML6; PRDM16-DT; LINC01346; LOC105376674; MIR6859-2; AURKAIP1; LOC105378586; RNU6-1100P; MIR5697; LOC105376691; LOC105378606; LOC100129776; SMIM1; WBP1LP7; LINC01777; MTATP6P1; UBE2J2; CEP104; VWA1; SLC25A33; CAMTA1-AS2; TTLL10; RNF207; PLCH2; PLEKHN1; SPSB1; ACTRT2; GPR153; ZBTB48; RN7SL731P; DFFA; LINC02593; SSU72; CHD5; RPL39P12; LOC100288175; C1orf127; FBXO6; MIR4251; KLHL17; LINC02606; MIR4689; LOC100288069; LINC01409; UBIAD1; LOC105378600; KCNAB2; GNB1-DT; MTCO2P12; HES3; RPL26P7; SNORD128; LOC112268219; TUBB8P11; RPL27P3; RPL7P11; HES5; MASP2; RPL23AP21; EXOSC10; C1orf174; DDX11L17; RN7SL574P; RNU6-731P; RER1; GABRD; THAP3; RNU6-304P; UTS2; DFFB; MTCO3P12; INTS11; ICMT; MTCO1P12; LOC105378601; LOC105376686; PEX10; LOC105376689; RNU1-7P; LOC105378604; PIK3CD-AS2; MMEL1-AS1; LOC105376682; MIR6808; HES4; MRPL20; LOC107984904; LOC102723897; LINC01770; MIR200A; TAS1R1; RNU6-991P; GPR157; AJAP1; MMEL1; MIR34A; PUSL1; TNFRSF4; FAM41C; ACOT7; H6PD; PRKCZ-AS1; OR4F16; LOC105378598; RNU1-8P; LOC100132287; ATAD3B; MAD2L2; CDK11B; TNFRSF14-AS1; TTC34; PRXL2B; CCDC27; TMEM201; TMEM274P; SEPTIN14P13; CFL1P6; PERM1; TNFRSF18; EEF1DP6; LINC01134; PLEKHG5; DRAXIN; CAMTA1-AS1; CPTP; TNFRSF14; LINC01342; LOC105378589; FAM87B; LOC105376737; NMNAT1; LOC107984912; LOC107984915; ANGPTL7; LOC107985728; ATAD3A; SLC2A7; SKI; LOC112268260; FAAP20; LOC107984872; ENO1; TMEM88B; LOC102724429; KLHL21; NOL9; MIB2; HES2; RNU6-828P; FNDC10; RPL9P11; SLC35E2A; CFAP74; SRM; DISP3; MIR429; NADK; TP73; RERE-AS1; LOC100288379; LINC02781; RN7SKP269; LOC105378947; RPL22; MTND1P23; MXRA8; MTOR; RNF207-AS1; LOC105376740; TPRG1L; LZIC; LOC105376717; GFOD3P; LOC112268220; LOC105378948; C1QTNF12; MIR12136; DNAJC11; CICP3; RPL23AP24; FBXO44; LOC100129534; PRDM16; RPL7AP18; TNFRSF25; PGD; CDK11A; LOC107984850; NDUFB4P8; UBE2V2P3; LOC100420339; TTLL10-AS1; LOC112268218; SLC2A5; LINC00115; ENO1-AS1; LOC112268261; TNFRSF9; MTND2P28; LOC105378593; WASH9P; LINC02782; LOC107984913; LOC105378599; ACAP3; DVL1; TARDBP; MTCYBP45; PIK3CD; LOC107985729; See more...

Location information:

Clinical significance:

ID:: 49579709

variant

12.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: PRKCZ-DT; RNU6-731P; LINC01646; LOC105376739; MIR4689; RPL27P3; GABRD; KCNAB2; GNB1-DT; LOC112268219; RN7SL731P; PLOD1; SLC35E2B; MIR6729; CASZ1; HES3; CHD5; SNORD167; EXOSC10; RN7SL574P; MMEL1-AS1; RNU1-7P; LOC100996583; TUBB8P11; ZBTB48; LOC100288175; LOC105376682; MIR4632; RPL21P21; MMP23A; CTNNBIP1; ARHGEF16; LINC02780; ISG15; LOC107984911; LRRC47; KIAA2013; LOC105378608; RERE; PHF13; MIR200B; CAMTA1-DT; CAMTA1; SDF4; KIF1B; EXOSC10-AS1; CLSTN1; PER3; ATAD3C; RPL39P6; RPL37P9; LNCTAM34A; WRAP73; NOC2L; MIR34AHG; MIR551A; LINC01672; LOC284600; HMGN2P17; ANKRD65-AS1; LINC01786; TMEM52; PANK4; TMEM240; RNU6-291P; ANKRD65; VAMP3; UBE4B; CA6; MEGF6; LOC105378605; PIK3CD-AS1; TAS1R3; MORN1; LOC105376733; MIR6728; MRPL20-AS1; ICMT-DT; NPPA; FBXO44; SLC2A5; RN7SL657P; C1QTNF12; PRDM16; LINC01647; RNU6-37P; GFOD3P; TNFRSF9; LOC101060126; RNU5E-4P; NDUFB4P8; MTOR-AS1; LINC02782; LOC112268261; MTCYBP45; UBE2V2P3; PGAM1P11; RBP7; LOC107985729; TTLL10-AS1; RN7SL451P; DNAJC11; LOC105378599; C1orf159; LZIC; SBF1P2; LOC107985732; ACAP3; PIK3CD; RPL23AP19; CCNL2; RPL22; LINC01714; RN7SKP269; TPRG1L; FBXO2; LOC107984850; TP73-AS3; LOC105378602; LOC100129534; RPL7P7; LOC105376695; LOC105378948; DVL1; LOC105378590; LOC107984913; MZT1P1; LOC105378593; LOC100420339; C1orf167-AS1; RNF207-AS1; TARDBP; CLCN6; MFN2; SAMD11; LOC112268218; RNA5SP40; LINC01128; MIR7846; MIR6727; ENO1-AS1; MXRA8; RNU6-537P; NPHP4; RNF223; SLC45A1; CENPS-CORT; TRUND-NNN4-1; MMP23B; LINC01345; TNFRSF1B; MIR4252; LINC01770; CENPS; PEX14; RNU6-991P; PLEKHG5; PRKCZ-AS1; LOC105376735; MAD2L2; CORT; RN7SL614P; MMEL1; PRKCZ; GNB1; MIR200A; CCDC27; MIR6808; HSPE1P24; DFFB; H6PD; TMEM274P; TNFRSF4; ACOT7; ICMT; PEX10; HES4; ESPN; LOC107984904; PUSL1; ERRFI1; B3GALT6; ATAD3B; RPL23AP89; NPPA-AS1; LOC105378601; PIK3CD-AS2; INTS11; RNU6-304P; LOC107984915; MIIP; LOC105376712; LOC105376686; PARK7; AGTRAP; LOC105376689; LOC107985728; NOL9; GPR157; RNU1-8P; SKI; DRAXIN; RPL7AP18; LOC112268220; TNFRSF14-AS1; LOC105378604; CDK11B; CFL1P6; CFAP74; FNDC10; UTS2; LINC01342; TAS1R1; PERM1; LINC02781; CPTP; LOC107984872; FAM41C; TMEM88B; RN7SL649P; TP73; LINC01134; PRXL2B; LOC102724429; RNU6-828P; MIR34A; AJAP1; MIR429; RPL9P11; LOC107984912; LOC105378586; SRM; TNFRSF18; PGD; TMEM201; ANGPTL7; LOC105378598; SLC2A7; SLC35E2A; FAAP20; TNFRSF14; RNU5E-1; LOC105378589; LOC100129776; LOC105376717; KLHL21; LOC105376674; MTOR; MIB2; LOC105376740; C1orf167; ENO1; CAMTA1-AS2; NADK; MIR6726; GPR153; ATAD3A; LOC105378606; PRDM16-DT; RPL39P12; PLEKHN1; TNFRSF25; CDK11A; LOC100129381; HES2; LOC105376737; RNF207; MIR5697; AURKAIP1; NMNAT1; DISP3; LOC100288379; RERE-AS1; CAMTA1-AS1; LOC107984909; TTC34; RNU6-777P; TTLL10; RPL26P7; SLC25A33; PLCH2; SNORD128; LINC01777; EEF1DP6; VWA1; SPSB1; SMIM1; RER1; HES5; C1orf174; FBXO6; VPS13D; KLHL17; LOC105378600; MTHFR; RPL10P17; LOC105376691; SCNN1D; SSU72; ACTRT2; UBIAD1; MIR4251; C1orf127; LINC02606; LINC01346; CALML6; NPPB; TNFRSF8; MASP2; UBE2J2; RPL7P11; CEP104; THAP3; MRPL20; DFFA; LINC02593; AGRN; See more...

Location information:

Clinical significance:

ID:: 48462401

variant

13.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: VWA1; CEP104; RPL7P11; UBE2J2; TTLL10; SNORD128; LINC02593; TNFRSF8; SMIM1; LINC01346; NPPB; CALML6; SLC25A33; HES5; RPL26P7; AGRN; C1orf174; MASP2; ACTRT2; MTHFR; KLHL17; RER1; MIR4251; UBIAD1; C1orf127; SCNN1D; LINC02606; MRPL20; HES3; LOC105378600; RPL10P17; THAP3; FBXO6; LOC112268219; MIR6729; SSU72; DFFA; GNB1-DT; LINC01646; SLC35E2B; PLOD1; LNCTAM34A; PRKCZ-DT; RPL27P3; RNU6-731P; CASZ1; MIR4689; EXOSC10; LOC100288175; GABRD; CHD5; ISG15; LOC105376739; LOC107984911; ZBTB48; KCNAB2; RPL21P21; MIR4632; SNORD167; RNU1-7P; LOC100996583; MMEL1-AS1; LOC105376682; RN7SL574P; MMP23A; RN7SL731P; LINC01672; KIF1B; LOC284600; PER3; WRAP73; CAMTA1-DT; NOC2L; HMGN2P17; CLSTN1; RPL39P6; LRRC47; ARHGEF16; KIAA2013; EXOSC10-AS1; PHF13; CAMTA1; LOC105378608; RERE; LINC02780; SDF4; MORN1; UBE4B; MIR200B; CTNNBIP1; LOC105376733; MIR6728; TMEM52; PANK4; VAMP3; ANKRD65-AS1; LOC105378605; TAS1R3; RPL37P9; TMEM240; ICMT-DT; ANKRD65; MRPL20-AS1; PIK3CD-AS1; RNU6-291P; CA6; ATAD3C; MIR34AHG; MEGF6; MIR551A; LINC01786; TNFRSF9; LINC02782; MTOR-AS1; RBP7; PGAM1P11; RNU5E-4P; UBE2V2P3; MTCYBP45; NDUFB4P8; LOC101060126; LOC112268261; TTLL10-AS1; LOC107985729; SLC2A5; RN7SL657P; GFOD3P; C1QTNF12; FBXO44; NPPA; RNU6-37P; LINC01647; LINC01714; PRDM16; TPRG1L; RN7SKP269; RN7SL451P; RPL22; C1orf159; RPL23AP19; SBF1P2; LOC105378602; FBXO2; CCNL2; PIK3CD; LOC107985732; LOC105378593; DNAJC11; LOC105378599; TARDBP; ACAP3; LZIC; SAMD11; LOC105378590; MFN2; RPL7P7; LOC112268218; DVL1; LOC107984913; TP73-AS3; LOC105376695; MMP23B; LOC105378948; MZT1P1; LOC105376735; LOC100129534; CENPS; LOC100420339; NPHP4; MIR7846; C1orf167-AS1; MIR6727; CLCN6; RNF207-AS1; RNA5SP40; CENPS-CORT; ENO1-AS1; RNF223; MXRA8; SLC45A1; PRKCZ-AS1; PEX14; LINC01345; HSPE1P24; RNU6-537P; TRUND-NNN4-1; CORT; LINC01770; TMEM274P; MIR200A; H6PD; PLEKHG5; MIR4252; RNU6-991P; CCDC27; LOC105378604; LOC105376689; MMEL1; MIR6808; ERRFI1; RPL23AP89; LOC107984904; MAD2L2; PARK7; MIIP; RNU6-304P; ESPN; NPPA-AS1; LOC105376712; ATAD3B; ACOT7; TNFRSF4; PRKCZ; TNFRSF1B; RN7SL614P; PUSL1; LOC105378601; GNB1; ICMT; B3GALT6; LOC105376686; HES4; INTS11; MIR429; TP73; NOL9; PEX10; RPL7AP18; LOC112268220; DFFB; AGTRAP; LOC107984872; RNU1-8P; FNDC10; TMEM88B; LINC02781; CDK11B; TNFRSF14; RPL9P11; PERM1; SRM; TAS1R1; RNU5E-1; GPR157; LOC107985728; ENO1; PGD; MIR34A; MIB2; TMEM201; TNFRSF14-AS1; UTS2; PIK3CD-AS2; LOC107984915; LOC105378598; SKI; CFAP74; DRAXIN; LOC102724429; CFL1P6; CPTP; RNU6-828P; RN7SL649P; TNFRSF18; PLCH2; RERE-AS1; LOC105376740; LINC01777; LOC100288379; PRDM16-DT; SLC2A7; LOC105376737; AJAP1; FAAP20; LOC105376717; PRXL2B; LINC01342; MTOR; VPS13D; EEF1DP6; MIR5697; LOC105378606; LOC105376691; AURKAIP1; NADK; LOC100129381; TTC34; RNU6-777P; LINC01134; CDK11A; ATAD3A; SPSB1; PLEKHN1; LOC100129776; RPL39P12; RNF207; SLC35E2A; KLHL21; TNFRSF25; DISP3; MIR6726; LOC105376674; LOC107984912; ANGPTL7; LOC105378586; LOC105378589; CAMTA1-AS1; NMNAT1; LOC107984909; CAMTA1-AS2; HES2; GPR153; C1orf167; See more...

Location information:

Clinical significance:

ID:: 54355922

variant

14.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: VPS13D; PRAMEF30P; RPL9P11; SRM; BRWD1P1; MTOR; LOC105376737; ENO1; CD24P1; PRAMEF33; PRAMEF20; CAMTA1-AS1; SNORA59A; RNU5E-1; NMNAT1; CELA2A; PRAMEF25; LOC107984912; LOC105376717; DRAXIN; LOC105376740; PRAMEF26; AGTRAP; LOC107984915; KLHL21; ANGPTL7; NOL9; RERE-AS1; RSC1A1; RPL7AP18; PGD; DDI2; LOC105378612; HES2; RN7SL649P; SLC2A7; UBE4B; RNU6-828P; TMEM201; SCARNA21B; RPL21P21; TNFRSF25; DISP3; LOC105376756; MIR4632; MIR6728; PRAMEF27; VAMP3; PRAMEF15; PHF13; LOC105376739; MFFP1; LOC105376759; CA6; CTNNBIP1; PER3; EXOSC10-AS1; LNCTAM34A; KIAA2013; CAMTA1-DT; CASZ1; KAZN-AS1; PRAMEF6; LINC01672; EFHD2-AS1; RNU6-1072P; KIF1B; CAMTA1; FBLIM1; TBCAP2; RNU1-7P; RNA5SP41; LINC02606; HNRNPCL1; ZBTB48; RPL12P14; PRAMEF2; RN7SL731P; TNFRSF8; RPL27P3; UBIAD1; C1orf127; PRAMEF32P; RPL26P7; RNU6-731P; MASP2; NPPB; RPL7P11; MIR6729; TMEM51; PLOD1; SNORD128; EXOSC10; PRAMEF13; LINC01784; MTHFR; PLEKHM2; RPL10P17; AADACL4; THAP3; CHCHD2P6; FBXO6; RN7SKP269; PRAMEF1; LOC107984913; UBE2V2P3; PRAMEF4; RNU6-1265P; FBXO44; CFAP107; PRAMEF29P; SLC2A5; LINC02766; HNRNPCL2; LOC112268261; ENO1-AS1; LOC101060126; LOC105376767; MTCYBP45; PRAMEF28P; TNFRSF9; AGMAT; MFN2; TARDBP; CELA2B; LZIC; DNAJC11; C1orf167-AS1; RNU5E-4P; PIK3CD-AS1; FBXO2; SBF1P2; ZBTB2P1; PIK3CD; MIR7846; PRAMEF5; LOC105376733; PRAMEF10; PRAMEF14; NPPA; DNAJC16; RERE; SLC25A34; LINC01714; PRAMEF18; RNU6-37P; CASP9; MTOR-AS1; HMGN2P17; PGAM1P11; RPL39P6; RBP7; CTRC; RNU7-179P; HNRNPCL4; AADACL3; LINC01647; MIR34AHG; CLSTN1; RPL37P9; KAZN; LOC107985469; LOC102724856; LOC105376689; RN7SL451P; RNU6-304P; PRAMEF9; DHRS3; PIK3CD-AS2; RPL23AP19; LOC107984918; GPR157; RNU6-291P; PRAMEF8; MIIP; TMEM274P; TAS1R1; SLC25A34-AS1; H6PD; RNU6-991P; PRAMEF34P; RNU1-8P; MAD2L2; CFL1P6; PRAMEF12; UTS2; PLEKHG5; ACOT7; CENPS; MZT1P1; PEX14; LOC105376735; ESPN; RN7SL614P; ERRFI1; PRAMEF7; LOC105376712; PRAMEF35P; LRRC38; TNFRSF1B; MIR34A; RPL23AP89; PRAMEF19; PRAMEF11; RNU6-771P; MIR4252; TMEM51-AS1; TMEM82; RNA5SP40; FHAD1; CLCN6; RNU6-537P; NPPA-AS1; SLC45A1; PRAMEF31P; TRUND-NNN4-1; TMEM51-AS2; RPL7P7; HSPE1P24; CORT; PRAMEF36P; LOC105376695; RNU6-777P; PRAMEF17; RNU6ATAC18P; LOC105376691; FHAD1-AS1; MIR5697; CENPS-CORT; HNRNPCL3; MIR6730; LOC107985467; PARK7; PRDM2; LOC100129776; PDPN; C1orf167; EFHD2; CAMTA1-AS2; DFFA; SPSB1; SLC25A33; See more...

Location information:

Clinical significance:

ID:: 48468838

variant

15.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: VAMP3; CTNNBIP1; ICMT-DT; CA6; LOC105378605; UBE4B; LOC107984911; LINC02780; PANK4; ANKRD65; TMEM52; ANKRD65-AS1; PHF13; RERE; LOC105378608; PIK3CD-AS1; RPL37P9; MMP23A; MORN1; SNORD167; MEGF6; CAMTA1-DT; LINC01786; TAS1R3; SLC35E2B; LOC100996583; MIR6728; SDF4; PER3; LOC284600; MIR551A; ARHGEF16; LINC01672; LNCTAM34A; PRKCZ-DT; CAMTA1; WRAP73; NOC2L; RN7SL657P; C1QTNF12; LOC105378599; LINC01714; TMEM240; ACAP3; MIR200B; MIR34AHG; RN7SKP269; RPL23AP19; ATAD3C; MRPL20-AS1; PIK3CD; RPL22; LOC105378602; C1orf159; CCNL2; CLSTN1; LOC107985732; TTLL10-AS1; RBP7; NDUFB4P8; RN7SL451P; LRRC47; PGAM1P11; HMGN2P17; GFOD3P; LOC100129534; LOC105378948; LOC107984913; DVL1; MXRA8; NPHP4; PRDM16; TPRG1L; MMP23B; RNF207-AS1; LZIC; DNAJC11; RNF223; SLC45A1; LOC107985729; LINC02782; ENO1-AS1; LOC112268218; SLC2A5; LOC112268261; LOC105378590; LOC100420339; LOC105378593; TNFRSF9; SAMD11; LINC01345; RPL7P7; RNA5SP40; DFFB; MIR6808; RNU6-991P; LOC105376712; MIR200A; LOC105378604; GNB1; MZT1P1; ERRFI1; PARK7; RNU6-304P; LOC107984904; MIR6727; LOC105376689; ESPN; INTS11; ACOT7; B3GALT6; PUSL1; PRKCZ; ATAD3B; PLEKHG5; CCDC27; TRUND-NNN4-1; LOC105376695; TP73-AS3; MIR4252; TMEM274P; H6PD; MMEL1; PEX10; TNFRSF4; CDK11B; ENO1; RPL9P11; LOC105376686; TNFRSF14; TMEM201; LOC105378601; UTS2; LOC112268220; MIR34A; PRXL2B; RPL7AP18; LOC107985728; TAS1R1; ICMT; CFAP74; HES4; PRKCZ-AS1; LOC105378598; AJAP1; FNDC10; LINC01770; CPTP; LINC02781; TNFRSF14-AS1; AURKAIP1; CAMTA1-AS1; PERM1; ATAD3A; RNU1-8P; TNFRSF18; SKI; PIK3CD-AS2; EEF1DP6; GPR157; TTC34; TP73; PLCH2; LINC01134; RNU6-828P; MIR429; RERE-AS1; LOC107984909; LOC100288379; NOL9; SLC35E2A; LOC107984912; HES2; TMEM88B; LOC107984872; LOC100129381; CDK11A; TNFRSF25; CAMTA1-AS2; LOC102724429; LOC107984915; NMNAT1; LINC01342; PRDM16-DT; LOC105376717; LOC105376674; LOC105378589; NADK; MIB2; LOC100129776; CALML6; KLHL21; AGRN; LINC01346; LOC105378586; SLC2A7; FAAP20; RNF207; GPR153; SCNN1D; LOC105378600; KLHL17; LINC02593; MRPL20; THAP3; SPSB1; RPL39P12; LOC105376691; LOC105378606; RPL7P11; PLEKHN1; VWA1; SMIM1; UBE2J2; MIR5697; HES5; LINC01777; CEP104; SLC25A33; MIR6726; KCNAB2; RPL27P3; ISG15; SSU72; RPL21P21; CHD5; TTLL10; LINC02606; GNB1-DT; MIR4689; LINC01646; RN7SL574P; RNU1-7P; LOC105376682; MMEL1-AS1; SNORD128; HES3; GABRD; ACTRT2; RPL26P7; LOC100288175; LOC112268219; ZBTB48; MIR4251; RER1; C1orf174; RNU6-731P; See more...

Location information:

Clinical significance:

ID:: 53680356

variant

16.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: PRAMEF2; RN7SL731P; C1orf127; CHD5; MASP2; ZBTB48; TNFRSF8; RPL26P7; RPL7P11; LINC02606; HNRNPCL1; RPL27P3; MIR4689; UBIAD1; FBXO6; NPPB; EXOSC10; AADACL4; THAP3; LINC01784; SNORD128; RPL10P17; LOC105376682; UTS2; LOC105376686; RNU6-304P; MIIP; LOC105376689; MTHFR; NPPA-AS1; ICMT; PRAMEF12; RNU6-991P; PIK3CD-AS2; PRAMEF34P; RNU1-8P; GPR157; PEX14; H6PD; TMEM274P; RPL23AP89; CFL1P6; MAD2L2; AJAP1; PLEKHG5; ACOT7; TAS1R1; NMNAT1; LOC102724429; PRAMEF30P; RPL9P11; SRM; MIR34A; SNORA59A; CAMTA1-AS1; ANGPTL7; RNU5E-1; PRAMEF25; LOC107984912; DRAXIN; LOC105376717; RPL7AP18; ENO1; AGTRAP; LOC107984915; LOC105376740; LINC02781; SLC2A7; MTOR; NOL9; TNFRSF25; RN7SL649P; PGD; TMEM201; DISP3; HES2; RNF207-AS1; RNU6-828P; RERE-AS1; RPL22; PRAMEF1; RN7SKP269; FBXO44; LINC01714; PRAMEF29P; MTCYBP45; LOC112268261; PRAMEF4; PRAMEF28P; TNFRSF9; TARDBP; LZIC; C1orf167-AS1; MIR7846; UBE2V2P3; RNU5E-4P; SLC2A5; LOC101060126; DNAJC11; PIK3CD; LINC02782; ENO1-AS1; SBF1P2; MFN2; HNRNPCL2; LINC02766; ESPN; ERRFI1; MIR4252; PARK7; LOC105376695; PRAMEF35P; TNFRSF1B; SLC45A1; TRUND-NNN4-1; CORT; RPL7P7; LOC105376712; MZT1P1; LOC105376735; LOC107984913; CFAP107; RN7SL614P; CLCN6; PRAMEF7; CENPS; HSPE1P24; NPHP4; RNA5SP40; RNU6-537P; CENPS-CORT; PRAMEF27; PRAMEF11; VAMP3; MIR4632; MIR6728; RPL21P21; RNU6-731P; EXOSC10-AS1; KCNAB2; KIAA2013; HNRNPCL3; CTNNBIP1; UBE4B; PRAMEF6; CASZ1; PHF13; LOC105376739; LINC01672; LINC01646; MIR6729; HES3; LNCTAM34A; PLOD1; RNU1-7P; LOC107984911; RNU6-1072P; PER3; KIF1B; ICMT-DT; CA6; CAMTA1-DT; FBXO2; LOC105376733; PIK3CD-AS1; NPPA; RERE; LINC01647; RNU6-37P; PGAM1P11; HMGN2P17; RPL37P9; RBP7; PRAMEF10; CAMTA1; RN7SL451P; RNU6-291P; MTOR-AS1; AADACL3; DHRS3; RNU6ATAC18P; VPS13D; MIR5697; CLSTN1; RPL39P6; LOC105376691; RPL23AP19; MIR34AHG; LOC100129776; MIR6730; KLHL21; SLC25A33; SPSB1; CAMTA1-AS2; C1orf167; RNU6-777P; GPR153; LOC105376737; DFFA; RNF207; See more...

Location information:

Clinical significance:

ID:: 48448763

variant

17.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: NPPA-AS1; PARK7; LOC105376689; HSPE1P24; ICMT; TRUND-NNN4-1; ESPN; RPL7P7; RNU6-304P; CORT; RN7SL614P; TNFRSF1B; MZT1P1; LOC105376735; PEX14; ERRFI1; PLEKHG5; LOC105376712; RPL23AP89; MIR4252; RNU6-991P; PRAMEF34P; H6PD; TMEM274P; CENPS-CORT; MAD2L2; ACOT7; C1orf127; SLC25A33; RPL7P11; LOC105376691; NPPB; UBIAD1; MASP2; RPL10P17; MIR6730; MTHFR; FBXO6; THAP3; DFFA; SPSB1; VPS13D; SNORA59A; PRAMEF30P; NMNAT1; RNU6ATAC18P; LOC105376717; SRM; RNU6-777P; LOC105376737; MIR5697; LOC107984912; DRAXIN; PRAMEF25; ANGPTL7; CAMTA1-AS1; SLC2A7; LOC100129776; MTOR; LOC105376740; KLHL21; CAMTA1-AS2; RERE-AS1; C1orf167; GPR153; HES2; RNU6-828P; TNFRSF25; RNF207; DISP3; LOC105376733; MIR6728; ICMT-DT; PIK3CD-AS1; CTNNBIP1; CA6; EXOSC10-AS1; KIAA2013; LOC107984911; PHF13; UBE4B; CAMTA1-DT; RERE; VAMP3; CASZ1; LNCTAM34A; LINC01672; RPL37P9; CAMTA1; CLSTN1; KIF1B; PER3; MIR4632; RPL39P6; LINC02606; HNRNPCL1; RNU6-291P; PRAMEF27; KCNAB2; RNU6-731P; ZBTB48; PRAMEF2; RN7SL731P; RPL26P7; CHD5; RPL21P21; MIR4689; SNORD128; LOC105376739; HES3; PRAMEF6; EXOSC10; MIR6729; LINC01784; RPL27P3; AADACL4; TNFRSF8; PLOD1; PRAMEF35P; LZIC; RNF207-AS1; RNU1-7P; LOC105376682; CFAP107; RNU6-1072P; SLC45A1; LOC112268261; C1orf167-AS1; PRAMEF7; CENPS; RNU6-537P; CLCN6; RNA5SP40; TNFRSF9; PRAMEF28P; UBE2V2P3; PRAMEF11; LINC02782; LOC105376695; LOC107984913; ENO1-AS1; FBXO2; TARDBP; PRAMEF10; RPL22; HNRNPCL3; RN7SKP269; FBXO44; NPHP4; RNU6-37P; MFN2; MIR7846; PRAMEF29P; NPPA; PGAM1P11; LOC101060126; HMGN2P17; SLC2A5; LINC01714; RNU5E-4P; PRAMEF1; AADACL3; MTOR-AS1; RN7SL451P; DNAJC11; PRAMEF4; MIR34AHG; LINC02766; RBP7; UTS2; PRAMEF12; MTCYBP45; ENO1; LOC102724429; AGTRAP; PIK3CD-AS2; LINC01647; RNU5E-1; LOC105376686; PIK3CD; DHRS3; SBF1P2; LOC107984915; RPL23AP19; RNU1-8P; GPR157; CFL1P6; RN7SL649P; TAS1R1; NOL9; TMEM201; RPL7AP18; MIR34A; RPL9P11; MIIP; LINC02781; PGD; See more...

Location information:

Clinical significance:

ID:: 48466799

variant

18.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: LINC01647; RNU6-37P; RN7SKP269; NPPA; PRAMEF10; RPL22; MIR34AHG; LINC01714; RN7SL451P; FBXO2; CLSTN1; PIK3CD; RBP7; RPL23AP19; SBF1P2; LOC101060126; DHRS3; PRAMEF4; MTCYBP45; PGAM1P11; AADACL3; TNFRSF9; RNU5E-4P; MTOR-AS1; HMGN2P17; SLC2A5; LOC107984913; CFAP107; SLC45A1; FBXO44; RNU6-537P; DNAJC11; RNF207-AS1; PRAMEF1; LINC02766; C1orf167-AS1; LZIC; ENO1-AS1; MFN2; MIR7846; PRAMEF11; UBE2V2P3; LINC02782; TARDBP; LOC112268261; NPHP4; CLCN6; LOC105376695; PLEKHG5; TNFRSF1B; TMEM274P; MIR4252; CORT; TRUND-NNN4-1; RPL7P7; ESPN; RNU6-991P; PEX14; NPPA-AS1; HSPE1P24; LOC105376712; CENPS; MZT1P1; RN7SL614P; LOC105376689; LOC105376735; PARK7; RNA5SP40; RNU6-304P; ERRFI1; CENPS-CORT; ACOT7; H6PD; MAD2L2; PIK3CD-AS2; RNU1-8P; ENO1; MIIP; RPL23AP89; RNU5E-1; CFL1P6; TMEM201; RPL9P11; ICMT; UTS2; MIR34A; PRAMEF12; LOC105376686; RPL7AP18; TAS1R1; PGD; GPR157; LOC105376740; ANGPTL7; RN7SL649P; LINC02781; LOC107984915; LOC105376737; LOC107984912; SLC2A7; MTOR; CAMTA1-AS1; DRAXIN; LOC105376717; AGTRAP; NMNAT1; VPS13D; PRAMEF30P; SRM; TNFRSF25; CAMTA1-AS2; LOC102724429; C1orf167; NOL9; KLHL21; RNU6-777P; LOC100129776; HES2; RNU6-828P; MIR6730; SNORA59A; RERE-AS1; DISP3; RPL7P11; MIR5697; LOC105376691; NPPB; SLC25A33; RNU6ATAC18P; UBIAD1; RPL10P17; MASP2; MTHFR; GPR153; RPL26P7; RNU6-731P; DFFA; THAP3; SPSB1; MIR4632; TNFRSF8; RNF207; RPL27P3; AADACL4; ZBTB48; RNU1-7P; LINC02606; HNRNPCL1; RPL21P21; LOC105376682; CHD5; PRAMEF2; KCNAB2; MIR4689; HES3; RERE; MIR6729; LINC01784; EXOSC10-AS1; PLOD1; LOC105376739; RN7SL731P; KIAA2013; FBXO6; CASZ1; C1orf127; CAMTA1; PHF13; CA6; VAMP3; EXOSC10; ICMT-DT; LOC105376733; CTNNBIP1; UBE4B; SNORD128; LINC01672; RNU6-291P; RPL37P9; PER3; LNCTAM34A; PIK3CD-AS1; LOC107984911; MIR6728; RPL39P6; KIF1B; CAMTA1-DT; See more...

Location information:

Clinical significance:

ID:: 48459625

variant

19.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: RNU6-771P; TMEM82; RNU6-537P; RPL22P3; RNA5SP40; CENPS-CORT; MFN2; TMEM51-AS2; PRAMEF19; PRAMEF31P; FHAD1; CFAP107; HNRNPCL3; CLCN6; FBXO42; MZT1P1; LOC105376735; PRAMEF35P; LOC105376712; HSPE1P24; TNFRSF1B; PRAMEF36P; PRAMEF11; ARHGEF19; CORT; TMEM51-AS1; ANO7L1; PRAMEF7; LRRC38; CENPS; FHAD1-AS1; SRARP; PRAMEF8; KAZN; PRAMEF9; MIIP; RPL23AP89; FAM131C2P; MAD2L2; LOC102724856; NPPA-AS1; SPATA21; PRAMEF12; PRAMEF34P; PIK3CD-AS2; CFL1P6; GPR157; RN7SL614P; H6PD; EPHA2; TMEM274P; SLC25A34-AS1; PEX14; MIR34A; RPL9P11; CELA2A; RN7SL649P; SNORA59A; PRAMEF26; SRM; TMEM201; PRAMEF30P; CD24P1; CLCNKA; RNU6-828P; SZRD1; PGD; RSC1A1; BRWD1P1; DISP3; SCARNA21B; RPS16P1; PRAMEF20; PRAMEF25; LOC105376740; MTOR; LOC105378612; LOC107984918; AGTRAP; RNU5E-1; ANGPTL7; DRAXIN; EFHD2; PRAMEF33; NMNAT1; DFFA; VPS13D; SPSB1; RNU6ATAC18P; PRDM2; RNU6-777P; SPEN; LOC107985467; MIR5697; PDPN; C1orf167; CPLANE2; LOC105376717; DDI2; SLC25A33; EPHA2-AS1; LOC105376737; C1orf127; PRAMEF17; RPL12P14; HSPB7; MIR6730; PRAMEF2; LINC02606; FBXO6; LINC01784; HNRNPCL1; EXOSC10; RN7SL731P; RPL10P17; NPPB; RPL26P7; TNFRSF8; MTHFR; UQCRHL; UBIAD1; MASP2; PRAMEF13; TMEM51; PRAMEF32P; RNU6-1072P; UBE4B; PLEKHM2; MFFP1; RPL21P21; LOC105376759; EXOSC10-AS1; MIR6729; RNA5SP41; NECAP2; FBLIM1; TBCAP2; LNCTAM34A; CASZ1; AADACL4; PRAMEF27; PLOD1; MIR4632; EFHD2-AS1; KAZN-AS1; PRAMEF15; LOC105376739; PRAMEF18; PRAMEF6; RNU6-291P; MIR34AHG; CLSTN1; KIF1B; RPL39P6; PIK3CD-AS1; DHRS3; KIAA2013; CTNNBIP1; LOC105376733; LOC105376756; RBP7; FAM131C; CTRC; FBXO2; RNU7-179P; HNRNPCL4; PRAMEF14; RNU6-37P; LINC01647; ZBTB17; LOC107985469; DNAJC16; AADACL3; CASP9; PRAMEF5; PGAM1P11; MIR7846; SLC25A34; CLCNKB; PRAMEF1; ZBTB2P1; PRAMEF10; C1orf167-AS1; SPEN-AS1; CHCHD2P6; LINC02766; SBF1P2; LOC105376767; CELA2B; HNRNPCL2; RN7SKP269; RNU6-1265P; TARDBP; PIK3CD; SLC2A5; PRAMEF29P; PRAMEF4; PRAMEF28P; LZIC; LOC101060126; MTCYBP45; RNU5E-4P; MTOR-AS1; NPPA; UBE2V2P3; MT1XP1; AGMAT; FBXO44; See more...

Location information:

Clinical significance:

ID:: 48460890

variant

20.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: PRAMEF31P; RNA5SP40; RNU6-537P; CENPS-CORT; HNRNPCL3; PRAMEF19; MAD2L2; TMEM82; PRAMEF36P; TMEM274P; RNU6-771P; CENPS; PEX14; LOC105376735; RN7SL614P; MZT1P1; FHAD1-AS1; FHAD1; PRAMEF34P; CORT; HSPE1P24; SLC25A34-AS1; TNFRSF1B; LOC105376712; LRRC38; NPPA-AS1; LOC102724856; PRAMEF35P; PRAMEF8; LOC107984918; RPL23AP89; PRAMEF12; CFL1P6; RSC1A1; TMEM201; PRAMEF20; PIK3CD-AS2; RPL9P11; KAZN; MIIP; RNU5E-1; RNU6-828P; PRAMEF9; RN7SL649P; DISP3; PGD; SCARNA21B; C1orf167; DDI2; LOC105378612; AGTRAP; PRAMEF25; LOC105376740; MTOR; LOC105376737; LOC105376717; SNORA59A; ANGPTL7; DRAXIN; SRM; NMNAT1; PRAMEF33; RNU6-777P; CD24P1; PRAMEF30P; CELA2A; VPS13D; PRAMEF26; BRWD1P1; DFFA; PDPN; MIR6730; EFHD2; PRDM2; MIR5697; NPPB; SLC25A33; LOC107985467; RNU6ATAC18P; PLEKHM2; LINC01784; UBIAD1; PRAMEF17; RNU6-1072P; MTHFR; MIR6729; AADACL4; PRAMEF13; PLOD1; KAZN-AS1; RPL10P17; MASP2; FBXO6; TNFRSF8; UQCRHL; RPL26P7; TMEM51; EXOSC10; RPL12P14; PRAMEF32P; HNRNPCL1; RN7SL731P; TBCAP2; PRAMEF2; RNU6-291P; LINC02606; CASZ1; KIF1B; PRAMEF6; LOC107985469; HNRNPCL4; C1orf127; LOC105376756; EXOSC10-AS1; RNA5SP41; PRAMEF15; LOC105376759; UBE4B; LOC105376739; CTNNBIP1; RPL21P21; EFHD2-AS1; MFFP1; KIAA2013; FBLIM1; MIR4632; PIK3CD; DHRS3; CLSTN1; MTOR-AS1; AADACL3; MTCYBP45; SBF1P2; LOC101060126; PRAMEF27; CASP9; RNU7-179P; SLC25A34; PRAMEF14; LINC01647; CTRC; PRAMEF29P; LOC105376733; PRAMEF18; NPPA; DNAJC16; PRAMEF10; PGAM1P11; RPL39P6; RBP7; MFN2; TMEM51-AS2; CELA2B; RNU6-37P; MIR7846; PRAMEF28P; FBXO2; AGMAT; RNU5E-4P; PRAMEF4; ZBTB2P1; TARDBP; PIK3CD-AS1; TMEM51-AS1; HNRNPCL2; LINC02766; CFAP107; RNU6-1265P; PRAMEF1; FBXO44; PRAMEF5; LZIC; LOC105376767; CHCHD2P6; CLCN6; C1orf167-AS1; UBE2V2P3; PRAMEF11; PRAMEF7; RN7SKP269; See more...

Location information:

Clinical significance:

ID:: 48455244

variant

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