mettl16[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:: METTL16

Location information:

Clinical significance:

ID:: 48464919

variant

2.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: METTL16

Location information:

Clinical significance:

ID:: 48459504

variant

3.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: LOC284009; METTL16; RN7SL33P

Location information:

Clinical significance:

ID:: 48469997

variant

4.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: METTL16; EIF4A1P9; RN7SL33P; PAFAH1B1; SAMD11P1

Location information:

Clinical significance:

ID:: 48455704

variant

5.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: SAMD11P1; PAFAH1B1; RN7SL33P; METTL16; EIF4A1P9

Location information:

Clinical significance:

ID:: 48476431

variant

6.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: EIF4A1P9; METTL16; PAFAH1B1; RN7SL33P

Location information:

Clinical significance:

ID:: 48476694

variant

7.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: RPS4XP17; SNORA67; RPA1; CTNS; CHRNE; ZZEF1; MIR3183; OR3A2; DERL2; POLR2A; GP1BA; LIAT1; SPNS3; OR1G1; OR1E1; YWHAE; ZMYND15; DOC2B; SLC52A1; SAT2; MIR6864; SPAG7; GLTPD2; OR1D3P; SNORD91A; MINK1; LOC101928044; GPS2; OR1D4; PRPF8; KIF1C-AS1; TRARG1; TNFSF12; RNA5SP434; OVCA2; BHLHA9; ATP1B2; CRK; TEKT1; MNT; TIMM22; TM4SF5; OR1P1; USP6; INPP5K; MYO1C; C1QBP; SNORD91B; LOC105371501; VPS53; SPEM2; MIR6776; SLC13A5; UBE2G1; LOC100128284; LINC02091; MIR4520-1; C17orf100; SOX15; NCBP3; OR1R1P; RNU6-955P; MCUR1P1; LOC105371481; LOC105371498; OR1E2; LOC107985017; SMG6; FXR2; LOC101927839; DVL2; FBXO39; MIR6865; LOC728392; TRPV3; ALOX15P1; ANKFY1; ZFP3; LOC107984988; LOC105371512; CAMTA2-AS1; EIF4A1; CTNS-AS1; PSMB6; CHRNB1; NUP88; SGSM2; LOC105371592; LOC105371509; RNU6-1264P; ZNF232; TP53; RABEP1; RPH3AL-AS1; SERPINF2; ZBTB4; YBX2; PFN1; SERPINF1; CAMKK1; ASGR2; RILP; ATP6V0CP1; INCA1; CLDN7; C17orf49; SLC25A11; ITGAE; LOC101927727; PHF23; RN7SL774P; HNRNPA1P16; HASPIN; OR3A1; MIR212; LOC105371430; LOC105371493; ZNF232-AS1; TMEM256; LOC642502; MIR195; LOC105371490; PITPNA; ALOX12P2; TMEM95; RNU7-31P; OR1D2; SPICP3; RNA5SP435; RN7SL784P; TLCD3A; AIPL1; SRR; SCIMP; PELP1-DT; MIR497; OR1D5; GABARAP; WSCD1; LOC100288728; LINC01975; RPS12P29; RPL23AP73; TNFSF13; SPATA22; TMEM102; C17orf107; OR1A1; LOC101927911; CYB5D2; WRAP53; SHBG; MRM3; RN7SL608P; KCTD11; SPNS2; HIC1; LOC100420060; ALOX12; BTF3P14; PELP1; LOC105371507; MIR497HG; RNF167; SLC16A13; SMYD4; PAFAH1B1; NLRP1; TMEM256-PLSCR3; RN7SL33P; NEURL4; SLC35G6; SAMD11P1; SPEM1; MIR1253; DLG4; ACADVL; RN7SL105P; CTDNEP1; SPEM3; MPDU1; LOC339166; NLGN2; KIAA0753; TXNDC17; MED31; BCL6B; ALOX15; LOC105371425; CLEC10A; ARRB2; GEMIN4; CLUH; RNASEK-C17orf49; TRPV1; RYKP1; RN7SL624P; PLD2; OR3A4P; TSR1; ASGR1; SPNS2-AS1; EIF4A1P9; PIMREG; P2RX5; TLCD2; SNORA48; ALOX12-AS1; LOC105371508; SENP3-EIF4A1; LOC105371485; ATP2A3; ZNF594; ZNF594-DT; NXN; RTN4RL1; MFSD1P1; GLOD4; LINC01996; MIR324; METTL16; DBIL5P; LOC100421332; WDR81; SLC2A4; PITPNA-AS1; MIS12; TAX1BP3; DHX33; LOC100422717; CCDC92B; ASPA; RAP1GAP2; PLSCR3; LOC105371505; LOC284009; SCARF1; P2RX1; LOC105371499; MPDU1-AS1; PITPNM3; TXNP4; OR3A3; SHPK; DPH1; ELP5; OR1E3; MED11; RPL21P125; MRPL14P1; LOC105371486; LOC101927864; OR1AC1P; SNORD10; SMTNL2; DHX33-DT; CD68; GGT6; EMC6; SENP3; SLC16A11; CAMTA2; RFLNB; TNK1; ABR; ABR-AS1; LOC105371480; MIR22HG; MIR132; KIF1C; EIF5A; LOC105371483; CXCL16; XAF1; ACAP1; MYBBP1A; OR1A2; MIR22; RPAIN; TNFSF12-TNFSF13; VMO1; P2RX5-TAX1BP3; OR3A5P; FGF11; RPL7AP64; RPH3AL; SLC43A2; ENO3; MIR4520-2; RNASEK; TRUND-NNN6-1; See more...

Location information:

Clinical significance:

ID:: 48476368

variant

8.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: LOC105371592; CAMKK1; INCA1; SERPINF2; RPH3AL-AS1; MIR22HG; LOC105371486; PFN1; RILP; SERPINF1; PSMB6; RPH3AL; LOC105371509; DPH1; ZNF232; LOC107984988; ANKFY1; NUP88; ATP6V0CP1; CTNS-AS1; LOC101927727; ZFP3; CAMTA2-AS1; SRR; SLC25A11; WSCD1; RPL23AP73; OR1D5; TLCD3A; SCIMP; RNU7-31P; RN7SL784P; SPICP3; HASPIN; LOC105371493; PITPNA; ZNF232-AS1; OR1D2; LOC642502; ALOX12P2; LOC105371430; SMYD4; RN7SL774P; LOC100288728; LOC105371490; OR1A1; RNA5SP435; RN7SL105P; LINC01975; RPS12P29; SAMD11P1; OR3A1; PAFAH1B1; INPP5K; RNU6-955P; RNF167; LOC105371481; PELP1; BTF3P14; LOC100420060; HIC1; CYB5D2; RN7SL608P; LOC105371507; NLRP1; SPNS2; MRM3; OVCA2; C17orf107; SPATA22; RNA5SP434; MNT; LOC101927911; ALOX15P1; FBXO39; RN7SL33P; TAX1BP3; P2RX5; KIAA0753; CLUH; ARRB2; LOC105371508; LOC105371505; EIF4A1P9; NXN; TSR1; LOC105371485; LOC339166; OR3A4P; PITPNA-AS1; LOC105371425; RN7SL624P; MIR1253; ATP2A3; TXNDC17; SPNS2-AS1; TRPV1; PLD2; EMC6; MFSD1P1; ABR-AS1; LOC100421332; P2RX1; AIPL1; PELP1-DT; SCARF1; METTL16; RAP1GAP2; DHX33; RPL21P125; MRPL14P1; DBIL5P; OR1E3; OR3A3; SHPK; RTN4RL1; ZNF594; LOC100422717; MIS12; ZNF594-DT; LINC01996; HNRNPA1P16; CCDC92B; WDR81; PITPNM3; TXNP4; LOC284009; ASPA; MIR212; CAMTA2; GLOD4; MIR22; MIR132; KIF1C; SPNS3; LOC105371499; MIR4520-2; SMTNL2; LOC105371480; CXCL16; LOC101927864; SLC43A2; P2RX5-TAX1BP3; MED11; ENO3; DHX33-DT; MYBBP1A; GGT6; LOC105371483; OR1A2; OR3A5P; RFLNB; ABR; OR1D4; RPAIN; SNORD91A; ZMYND15; OR1AC1P; TLCD2; KIF1C-AS1; SLC52A1; RYKP1; XAF1; OR1E1; LIAT1; GP1BA; ALOX15; VMO1; ZZEF1; GEMIN4; OR3A2; CHRNE; RPA1; MED31; CTNS; MIR3183; PIMREG; RPS4XP17; MINK1; LOC101928044; DERL2; SPAG7; MIR6864; OR1D3P; OR1G1; YWHAE; VPS53; DOC2B; GLTPD2; LOC101927839; LOC105371501; OR1E2; C17orf100; MYO1C; C1QBP; LINC02091; LOC107985017; MIR4520-1; MIR6776; SNORD91B; OR1P1; PRPF8; SGSM2; SLC13A5; TEKT1; LOC100128284; RNU6-1264P; USP6; LOC728392; OR1R1P; TRPV3; SMG6; LOC105371498; TRARG1; MCUR1P1; MIR6865; NCBP3; TM4SF5; UBE2G1; RABEP1; TIMM22; BHLHA9; CRK; ITGAE; See more...

Location information:

Clinical significance:

ID:: 48479239

variant

9.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: CHRNE; SPNS2-AS1; OR3A4P; GEMIN4; ZZEF1; MIR3183; CTNS; KIF1C-AS1; LOC339166; SLC52A1; OR3A2; RPA1; ALOX15; OR1E1; LOC101928044; RYKP1; DOC2B; MFSD1P1; LOC100421332; TLCD2; OR1D3P; GLTPD2; MIR6864; MIR1253; SPAG7; YWHAE; RN7SL624P; LOC284009; TRPV1; PITPNA-AS1; TXNP4; METTL16; DBIL5P; LOC105371485; ARRB2; TAX1BP3; TSR1; CCDC92B; NXN; P2RX5; WDR81; LOC105371505; CLUH; LOC105371425; P2RX1; RPL21P125; PLD2; RAP1GAP2; EIF4A1P9; ATP2A3; EMC6; ASPA; GLOD4; ZNF594-DT; RN7SL774P; LINC01996; ZNF594; OR3A1; MIS12; HNRNPA1P16; MIR212; PITPNA; RTN4RL1; OR3A3; DHX33; SHPK; SCARF1; SCIMP; OR1E3; LOC100422717; SRR; MRPL14P1; OR1D5; PELP1-DT; ABR-AS1; TLCD3A; LOC105371499; LINC01975; CAMTA2; SPATA22; LOC642502; LOC105371493; ZNF232-AS1; HASPIN; LOC105371490; LOC105371430; SMYD4; LOC100420060; OR1D2; RNU7-31P; LOC105371507; PAFAH1B1; RN7SL784P; RN7SL33P; LOC100288728; SAMD11P1; RPS12P29; OR1A1; RNA5SP434; RN7SL105P; TRARG1; CRK; NLRP1; MNT; LOC101927911; BHLHA9; MRM3; CYB5D2; RN7SL608P; SPNS2; USP6; RNU6-955P; SNORD91B; OVCA2; MCUR1P1; HIC1; C17orf107; INPP5K; RNF167; MIR6776; LOC105371501; OR1P1; TRPV3; PELP1; SMG6; LOC105371481; CTNS-AS1; UBE2G1; LOC100128284; RABEP1; TM4SF5; SGSM2; VPS53; TIMM22; RPH3AL-AS1; ITGAE; LOC101927839; INCA1; NCBP3; ZFP3; LOC728392; LOC105371498; MYO1C; SERPINF2; C1QBP; OR1E2; LINC02091; OR1R1P; LOC105371486; SLC43A2; RPH3AL; LOC107984988; OR3A5P; MIR6865; CAMTA2-AS1; PSMB6; LOC105371592; ZNF232; DHX33-DT; RILP; SERPINF1; CAMKK1; MIR22HG; SLC25A11; MIR22; DPH1; ANKFY1; KIF1C; NUP88; ATP6V0CP1; LOC101927727; VMO1; OR1AC1P; DERL2; MIR132; PFN1; RPS4XP17; LIAT1; GGT6; RFLNB; P2RX5-TAX1BP3; ABR; OR1G1; LOC105371480; ENO3; SMTNL2; OR1A2; MINK1; LOC105371483; GP1BA; ZMYND15; MYBBP1A; SNORD91A; MED11; PRPF8; RPAIN; LOC101927864; SPNS3; CXCL16; OR1D4; See more...

Location information:

Clinical significance:

ID:: 48485901

variant

10.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: SRR; DBIL5P; SCARF1; CCDC92B; CAMTA2; LOC100421332; OR3A3; RPL21P125; SHPK; MIR212; LOC105371485; LOC105371425; TXNP4; RTN4RL1; MRPL14P1; LINC01996; LOC105371505; OR1E3; MIR1253; MIS12; METTL16; GLOD4; ZNF594; DHX33; PITPNA-AS1; MFSD1P1; ASPA; SPNS2-AS1; HNRNPA1P16; LOC284009; RN7SL33P; RN7SL624P; RNU6-955P; LOC100420060; OR1A1; LOC105371501; OR1D5; LOC105371481; TLCD3A; RPS12P29; MIR6776; SCIMP; SMYD4; LOC105371507; RN7SL608P; LOC101927911; PITPNA; OR3A1; LOC642502; HASPIN; OR1D2; C17orf107; SNORD91B; INPP5K; RNA5SP434; RNF167; SAMD11P1; LOC100288728; RN7SL784P; PELP1; PAFAH1B1; HIC1; MRM3; LOC105371490; CYB5D2; NLRP1; RNU7-31P; SPNS2; LOC105371430; RN7SL774P; BHLHA9; ZNF232-AS1; LOC105371493; OVCA2; SMG6; RN7SL105P; SPATA22; MYO1C; MNT; OR1R1P; VPS53; NCBP3; LOC105371486; C1QBP; LOC101927727; LOC728392; LOC105371592; ITGAE; INCA1; MCUR1P1; OR1E2; ATP6V0CP1; OR1P1; RABEP1; CTNS-AS1; DHX33-DT; UBE2G1; USP6; SGSM2; TM4SF5; LOC107984988; CRK; PFN1; TIMM22; TRPV3; RPH3AL-AS1; LOC105371498; TRARG1; CAMTA2-AS1; SERPINF2; RILP; LOC101927839; MIR132; LINC02091; MIR22; DPH1; ZNF232; VMO1; SERPINF1; CAMKK1; NUP88; ZFP3; KIF1C; RPH3AL; MIR22HG; ANKFY1; PSMB6; MIR6865; SNORD91A; OR1A2; SLC25A11; KIF1C-AS1; ZMYND15; MIR3183; OR1D4; SPNS3; LIAT1; ABR; RPAIN; CXCL16; MED11; MYBBP1A; ENO3; SLC43A2; GGT6; SMTNL2; OR1G1; LOC101928044; YWHAE; SPAG7; OR1AC1P; RFLNB; MINK1; TLCD2; LOC101927864; GP1BA; MIR6864; DOC2B; OR3A5P; P2RX5-TAX1BP3; RPA1; ZZEF1; CTNS; OR3A4P; ALOX15; SLC52A1; LOC105371480; GLTPD2; OR1D3P; GEMIN4; PRPF8; RPS4XP17; OR3A2; CHRNE; OR1E1; RYKP1; LOC105371483; NXN; TAX1BP3; ABR-AS1; RAP1GAP2; TSR1; DERL2; LOC100422717; EMC6; PELP1-DT; ARRB2; ZNF594-DT; LOC105371499; CLUH; EIF4A1P9; P2RX1; ATP2A3; P2RX5; WDR81; PLD2; TRPV1; LINC01975; See more...

Location information:

Clinical significance:

ID:: 50271737

variant

11.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: BHLHA9; MNT; TIMM22; LOC728392; MIR6865; SMG6; TRPV3; TRARG1; TM4SF5; CRK; RNU6-955P; MCUR1P1; UBE2G1; SGSM2; USP6; RABEP1; OR1P1; OVCA2; C1QBP; OR1E2; OR1R1P; MIR6776; MYO1C; LOC101927839; LOC105371501; VPS53; LOC105371481; NCBP3; LOC105371498; SNORD91B; HNRNPA1P16; LOC284009; ZNF594; CAMTA2; ASPA; GLOD4; PITPNA-AS1; TXNP4; RTN4RL1; ZNF594-DT; LINC01996; WDR81; DHX33; LOC105371499; LOC100422717; MIS12; CCDC92B; DBIL5P; METTL16; OR1E3; PELP1-DT; RAP1GAP2; SCARF1; MRPL14P1; OR3A3; SHPK; ABR-AS1; RPL21P125; LOC105371493; ZNF232-AS1; LOC105371430; P2RX1; OR3A1; RN7SL774P; RN7SL105P; HASPIN; LINC01975; RNU7-31P; LOC642502; MIR212; LOC105371490; OR1D2; PITPNA; RN7SL784P; TLCD3A; OR1D5; OR1A1; SCIMP; RPS12P29; LOC100288728; SRR; OR1D4; MIR6864; RPA1; PRPF8; OR3A2; LOC101928044; CHRNE; DERL2; RPS4XP17; ZZEF1; LIAT1; CTNS; MIR3183; SLC52A1; SPNS3; TLCD2; YWHAE; GLTPD2; GP1BA; OR1G1; KIF1C-AS1; OR1E1; SPAG7; MFSD1P1; OR1D3P; SPNS2-AS1; MINK1; GEMIN4; PLD2; ATP2A3; MIR1253; RN7SL624P; ALOX15; TRPV1; OR3A4P; TSR1; P2RX5; EMC6; LOC105371425; EIF4A1P9; LOC105371485; RYKP1; CLUH; ARRB2; ANKFY1; LOC107984988; SLC25A11; TAX1BP3; LOC101927727; LOC105371505; NXN; LOC100421332; SERPINF2; CAMTA2-AS1; ZFP3; NUP88; CTNS-AS1; SERPINF1; ATP6V0CP1; ZNF232; CAMKK1; INCA1; PSMB6; RPH3AL-AS1; RILP; PFN1; LOC105371592; DPH1; ZMYND15; MED11; ITGAE; RPH3AL; LOC101927864; OR3A5P; P2RX5-TAX1BP3; ENO3; DHX33-DT; SLC43A2; GGT6; OR1AC1P; SMTNL2; CXCL16; OR1A2; KIF1C; MIR132; LOC105371480; RPAIN; MIR22HG; SPATA22; LOC105371486; SNORD91A; RFLNB; RNA5SP434; ABR; MIR22; LOC105371483; NLRP1; VMO1; MYBBP1A; MRM3; C17orf107; HIC1; SPNS2; LOC105371507; SMYD4; SAMD11P1; INPP5K; PELP1; LOC101927911; CYB5D2; LOC100420060; PAFAH1B1; RN7SL608P; RNF167; RN7SL33P; See more...

Location information:

Clinical significance:

ID:: 48477150

variant

12.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: ARRB2; RYKP1; NXN; CLUH; TLCD2; OR1D3P; YWHAE; MFSD1P1; MIR1253; RN7SL624P; SPNS2-AS1; GEMIN4; TRPV1; LOC105371425; TAX1BP3; ALOX15; OR3A4P; P2RX5; DBIL5P; EIF4A1P9; SHPK; RPL21P125; ATP2A3; SCARF1; RAP1GAP2; LOC100422717; LOC105371485; TXNP4; EMC6; P2RX1; CCDC92B; TSR1; ABR-AS1; LOC105371499; ASPA; LOC284009; LINC01996; METTL16; GLOD4; OR3A3; PITPNA-AS1; RTN4RL1; WDR81; OR1D5; PELP1-DT; TLCD3A; MRPL14P1; OR1E3; OR1A1; LINC01975; LOC105371430; RPS12P29; MIR212; SRR; LOC100288728; LOC642502; LOC105371493; HNRNPA1P16; OR3A1; RN7SL774P; PITPNA; OR1D2; PAFAH1B1; HIC1; SMYD4; PELP1; LOC100420060; SAMD11P1; RN7SL33P; RN7SL105P; HASPIN; MRM3; LOC101927911; SPATA22; SPNS2; CYB5D2; LOC105371481; MIR6776; VPS53; UBE2G1; LOC105371490; LOC101927839; RNU6-955P; OR1E2; MCUR1P1; INPP5K; TIMM22; SNORD91B; BHLHA9; LOC105371498; OR1R1P; TRPV3; CRK; MNT; TRARG1; RNA5SP434; NCBP3; RN7SL608P; OVCA2; OR1P1; SERPINF1; SMG6; ITGAE; RPH3AL-AS1; SERPINF2; CTNS-AS1; ANKFY1; MYO1C; SGSM2; CAMKK1; LOC101927727; ABR; MIR22; LOC105371483; RILP; OR1A2; DPH1; RPH3AL; MED11; LOC107984988; MIR22HG; MIR132; SLC43A2; OR3A5P; LOC105371592; RFLNB; LOC105371486; OR1G1; MYBBP1A; CTNS; LOC105371480; PRPF8; SNORD91A; GGT6; OR1AC1P; MIR3183; ZZEF1; P2RX5-TAX1BP3; RPA1; OR3A2; RPS4XP17; OR1E1; SPNS3; CXCL16; LIAT1; OR1D4; SMTNL2; LOC101927864; See more...

Location information:

Clinical significance:

ID:: 48485134

variant

13.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: LOC105371430; LOC642502; MIR212; LOC105371493; RN7SL105P; HASPIN; OR3A1; LOC105371490; SAMD11P1; OR1D2; LINC01975; SRR; LOC100288728; OR1D5; OR1A1; PITPNA; LIAT1; TLCD3A; ZZEF1; MIR3183; RPA1; RPS4XP17; YWHAE; OR3A2; PRPF8; OR1E1; CTNS; OR1D3P; OR1G1; RYKP1; TLCD2; PITPNA-AS1; GEMIN4; MIR1253; LOC105371425; RN7SL624P; ATP2A3; TRPV1; TAX1BP3; NXN; P2RX5; CLUH; TSR1; EIF4A1P9; EMC6; LOC105371485; OR3A4P; CTNS-AS1; ANKFY1; LOC107984988; LOC101927727; SERPINF2; RPH3AL-AS1; RILP; P2RX5-TAX1BP3; OR3A5P; SLC43A2; SERPINF1; LOC105371592; CAMKK1; RPH3AL; MIR22HG; DPH1; MIR22; OR1AC1P; LOC105371480; OR1D4; SNORD91A; LOC101927864; OR1A2; LOC105371486; RFLNB; MIR132; ABR; LOC105371483; MNT; LOC101927911; CYB5D2; OVCA2; RN7SL33P; RNA5SP434; INPP5K; LOC100420060; PAFAH1B1; MRM3; RN7SL608P; SPATA22; SMYD4; CRK; HIC1; TIMM22; LOC105371481; BHLHA9; SMG6; MCUR1P1; TRARG1; MYO1C; OR1R1P; VPS53; SNORD91B; NCBP3; SGSM2; ITGAE; OR1P1; MIR6776; TRPV3; GLOD4; LOC101927839; ASPA; LOC100422717; LOC284009; OR1E2; P2RX1; ABR-AS1; DBIL5P; RTN4RL1; RPL21P125; WDR81; HNRNPA1P16; METTL16; CCDC92B; OR1E3; MRPL14P1; OR3A3; SHPK; RAP1GAP2; SCARF1; See more...

Location information:

Clinical significance:

ID:: 48483174

variant

14.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: OVCA2; RN7SL608P; MNT; LOC101927911; SMG6; SPATA22; MRM3; SNORD91B; BHLHA9; MIR6776; INPP5K; HIC1; RN7SL33P; PAFAH1B1; LOC101927864; SLC43A2; LOC105371481; LIAT1; RFLNB; ABR; OR1G1; P2RX5-TAX1BP3; OR3A5P; RPS4XP17; OR1D4; OR1AC1P; OR1A2; SNORD91A; LOC105371480; LOC105371483; CAMKK1; LOC105371486; MIR22HG; LOC105371592; RPH3AL; DPH1; LOC107984988; CTNS-AS1; LOC101927727; RILP; SERPINF1; SERPINF2; MIR132; CCDC92B; MIR22; DBIL5P; WDR81; LOC105371485; LOC105371425; TRPV1; RN7SL624P; MIR1253; PITPNA-AS1; EMC6; ATP2A3; RPL21P125; NXN; RAP1GAP2; P2RX5; TAX1BP3; TSR1; CLUH; OR3A4P; CTNS; RPA1; P2RX1; EIF4A1P9; MIR3183; GEMIN4; DOC2B; PRPF8; OR3A2; YWHAE; SMYD4; TLCD2; OR1E1; OR1D3P; LOC105371430; SAMD11P1; PITPNA; RN7SL105P; OR1D5; OR1A1; LOC105371490; LOC100288728; LOC642502; LOC105371493; HASPIN; OR1D2; SHPK; OR3A3; LOC284009; ASPA; HNRNPA1P16; GLOD4; MIR212; OR1E3; RTN4RL1; MRPL14P1; TLCD3A; METTL16; ABR-AS1; SCARF1; LOC100422717; OR3A1; SRR; OR1P1; CRK; TRARG1; TIMM22; SGSM2; ITGAE; OR1R1P; TRPV3; RPH3AL-AS1; VPS53; MCUR1P1; LOC101927839; OR1E2; NCBP3; MYO1C; LINC02091; See more...

Location information:

Clinical significance:

ID:: 48468054

variant

15.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: OR1P1; MRM3; RN7SL608P; LOC105371481; MIR6776; VPS53; SNORD91B; NCBP3; OR1R1P; INPP5K; MCUR1P1; OVCA2; TRPV3; TRARG1; SMG6; CRK; MNT; TIMM22; BHLHA9; LINC02091; SERPINF1; SGSM2; MYO1C; ITGAE; SERPINF2; LOC101927839; OR1E2; CTNS-AS1; RPH3AL-AS1; RPH3AL; SLC43A2; DPH1; OR3A5P; LOC105371486; LOC105371483; MIR22HG; RFLNB; LOC105371592; ABR; CAMKK1; MIR132; MIR22; OR1A2; RILP; LOC101927727; LOC107984988; LIAT1; RPS4XP17; P2RX5-TAX1BP3; OR1E1; LOC101927864; SNORD91A; OR1G1; LOC105371480; OR3A2; OR1D4; OR1AC1P; PRPF8; LOC105371425; MIR3183; OR3A4P; TLCD2; RPA1; NXN; CTNS; YWHAE; DOC2B; OR1D3P; GEMIN4; TRPV1; WDR81; OR3A3; PITPNA-AS1; RAP1GAP2; EIF4A1P9; LOC100422717; LOC105371485; SHPK; SCARF1; RPL21P125; ABR-AS1; EMC6; METTL16; LOC284009; CCDC92B; MIR1253; P2RX5; RN7SL624P; ASPA; ATP2A3; DBIL5P; CLUH; P2RX1; TAX1BP3; TSR1; MRPL14P1; OR1E3; OR1D5; OR1A1; SRR; OR1D2; RTN4RL1; GLOD4; PITPNA; HNRNPA1P16; LOC105371430; TLCD3A; MIR212; HIC1; LOC101927911; SMYD4; LOC105371493; OR3A1; LOC100288728; PAFAH1B1; RN7SL33P; SAMD11P1; SPATA22; HASPIN; LOC105371490; RN7SL105P; LOC642502; See more...

Location information:

Clinical significance:

ID:: 48456221

variant

16.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: RN7SL624P; LOC105371425; MIR1253; OR3A4P; NXN; TRPV1; GEMIN4; LOC105371485; CLUH; EIF4A1P9; TLCD2; SGSM2; LOC105371592; CTNS-AS1; RILP; LOC101927727; RPH3AL-AS1; SERPINF1; SERPINF2; RFLNB; RPH3AL; OR3A5P; SLC43A2; MIR22HG; LOC105371486; DPH1; LOC107984988; LOC105371480; MIR22; ABR; OR1A2; MIR132; LOC101927911; LOC105371483; MRM3; RN7SL105P; LOC105371490; SPATA22; SAMD11P1; RN7SL33P; SMYD4; PAFAH1B1; HIC1; OR1P1; CRK; MNT; BHLHA9; RN7SL608P; SMG6; TIMM22; OVCA2; OR1R1P; MYO1C; SNORD91B; TRARG1; TRPV3; LOC105371481; MCUR1P1; INPP5K; RTN4RL1; LOC101927839; OR1E2; METTL16; PITPNA-AS1; MIR6776; VPS53; WDR81; TSR1; GLOD4; DBIL5P; OR3A3; ASPA; LOC284009; SCARF1; PITPNA; CCDC92B; RAP1GAP2; OR1D2; ABR-AS1; LOC100422717; LOC642502; LOC105371493; OR3A1; MRPL14P1; LOC105371430; SHPK; HNRNPA1P16; MIR212; SRR; TLCD3A; LOC100288728; LOC101927864; LIAT1; OR1A1; OR1E3; MIR3183; OR1D5; OR1D3P; OR3A2; PRPF8; OR1D4; OR1E1; OR1G1; RPA1; RPS4XP17; OR1AC1P; YWHAE; SNORD91A; CTNS; See more...

Location information:

Clinical significance:

ID:: 48483621

variant

17.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: GEMIN4; OR3A2; OR3A4P; TLCD2; PRPF8; YWHAE; OR1D3P; MIR3183; OR1E1; RN7SL105P; RPA1; LOC105371430; OR3A1; LOC100288728; SAMD11P1; SRR; OR1A1; LOC642502; OR1D5; TLCD3A; SMYD4; PITPNA; OR1D2; LOC105371490; ASPA; LOC284009; HNRNPA1P16; SCARF1; ABR-AS1; OR3A3; OR1E3; MRPL14P1; CCDC92B; RTN4RL1; MIR212; GLOD4; METTL16; TRARG1; TIMM22; SNORD91B; OR1R1P; MYO1C; VPS53; LOC101927839; MCUR1P1; OR1E2; MIR6776; OR1P1; SGSM2; CRK; OVCA2; SMG6; MNT; BHLHA9; SPATA22; RN7SL33P; INPP5K; PAFAH1B1; LOC105371481; RN7SL608P; LOC101927911; HIC1; OR1AC1P; MRM3; OR1D4; LOC105371480; OR1G1; LOC105371483; ABR; SNORD91A; RFLNB; LOC101927864; OR1A2; RPS4XP17; OR3A5P; SLC43A2; MIR22; LIAT1; RILP; LOC101927727; RPH3AL-AS1; LOC105371592; LOC105371486; MIR132; SERPINF1; MIR22HG; LOC107984988; RPH3AL; SERPINF2; EIF4A1P9; TSR1; RN7SL624P; DPH1; NXN; CLUH; LOC105371485; LOC105371425; DBIL5P; MIR1253; WDR81; RAP1GAP2; PITPNA-AS1; See more...

Location information:

Clinical significance:

ID:: 48465643

variant

18.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: LINC01996; OR3A1; HNRNPA1P16; LOC105371499; ZNF594-DT; ASPA; RN7SL774P; LINC01975; CAMTA2; SCIMP; LOC100422717; OR1E3; SRR; PELP1-DT; OR1D5; OR3A3; SHPK; MED11; OR1AC1P; SNORD91A; ZMYND15; MYBBP1A; SPNS3; OR1D4; MINK1; OR1G1; P2RX5-TAX1BP3; ENO3; GGT6; SMTNL2; CXCL16; LOC101927864; GP1BA; ZZEF1; SPNS2-AS1; MFSD1P1; GLTPD2; OR3A2; CHRNE; KIF1C-AS1; OR1D3P; SPAG7; LOC100421332; SLC52A1; MIR6864; OR1E1; RYKP1; CTNS; OR3A4P; ALOX15; ITGAE; CTNS-AS1; NCBP3; OR1R1P; UBE2G1; MIR6865; LOC105371498; INCA1; LOC101927839; OR1E2; TM4SF5; SGSM2; ANKFY1; LOC107984988; SLC25A11; ZFP3; CAMTA2-AS1; PSMB6; ATP6V0CP1; CAMKK1; OR1A2; VMO1; OR3A5P; PFN1; ZNF232; KIF1C; SPATA22; LOC105371592; ZNF232-AS1; HASPIN; SAMD11P1; OR1A1; RPS12P29; LOC105371493; PAFAH1B1; LOC105371490; RN7SL33P; LOC100420060; RN7SL784P; LOC100288728; LOC101927911; RNA5SP434; TRPV3; USP6; C17orf107; OR1D2; LOC105371501; HIC1; MIR6776; RNF167; SPNS2; MNT; MCUR1P1; SMG6; OR1P1; RN7SL608P; LOC284009; RNU6-955P; SNORD91B; PELP1; RN7SL624P; EMC6; ZNF594; TSR1; CYB5D2; RPL21P125; RAP1GAP2; TAX1BP3; MIR1253; TXNP4; TRPV1; PLD2; ATP2A3; P2RX1; P2RX5; ARRB2; CLUH; EIF4A1P9; METTL16; CCDC92B; See more...

Location information:

Clinical significance:

ID:: 48484150

variant

19.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: LOC105371483; MIR132; MIR22; RILP; ABR; LOC101927727; OR1A2; RPH3AL; SLC43A2; LOC107984988; DPH1; LOC105371592; LOC105371486; MIR22HG; HIC1; RFLNB; PAFAH1B1; LOC100288728; LOC105371490; RN7SL33P; SAMD11P1; LOC642502; RN7SL105P; MRM3; SMYD4; LOC101927911; LOC105371481; MIR6776; VPS53; SNORD91B; MCUR1P1; SMG6; CRK; INPP5K; MNT; TIMM22; BHLHA9; TRARG1; OVCA2; OR1P1; RN7SL608P; RAP1GAP2; SCARF1; EIF4A1P9; CLUH; ABR-AS1; TSR1; MIR1253; LOC284009; RN7SL624P; CCDC92B; DBIL5P; WDR81; PITPNA-AS1; METTL16; MRPL14P1; LOC105371485; TLCD3A; SRR; OR1A1; OR1E3; OR1D5; HNRNPA1P16; LOC105371430; MIR212; OR1D2; GLOD4; PITPNA; RTN4RL1; LOC105371480; PRPF8; OR1D4; SNORD91A; OR1G1; LIAT1; LOC101927864; MIR3183; TLCD2; RPS4XP17; NXN; RPA1; GEMIN4; LOC105371425; YWHAE; DOC2B; MYO1C; LINC02091; LOC101927839; SERPINF2; SERPINF1; SGSM2; RPH3AL-AS1; See more...

Location information:

Clinical significance:

ID:: 48477121

variant

20.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: RN7SL608P; LOC101927911; CRK; MNT; BHLHA9; MRM3; SMG6; OVCA2; TRARG1; SNORD91B; INPP5K; HIC1; LOC105371481; MIR6776; LOC105371425; CCDC92B; MCUR1P1; DBIL5P; WDR81; LOC105371485; METTL16; PITPNA-AS1; MIR1253; LOC284009; RN7SL624P; EIF4A1P9; TSR1; CLUH; RAP1GAP2; NXN; PITPNA; RTN4RL1; MIR212; GLOD4; HNRNPA1P16; ABR-AS1; TLCD3A; SRR; OR1D5; SCARF1; MRPL14P1; LOC101927864; RPS4XP17; LIAT1; SNORD91A; PRPF8; LOC105371483; LOC105371480; ABR; RPA1; GEMIN4; MIR3183; YWHAE; TLCD2; SGSM2; RPH3AL-AS1; LOC101927839; TIMM22; SERPINF2; MYO1C; VPS53; SLC43A2; LOC107984988; RPH3AL; DPH1; LOC101927727; MIR22HG; LOC105371592; MIR132; RFLNB; LOC105371486; RILP; SERPINF1; OR1D2; SMYD4; LOC105371490; LOC105371430; MIR22; SAMD11P1; RN7SL105P; LOC642502; RN7SL33P; PAFAH1B1; See more...

Location information:

Clinical significance:

ID:: 48483081

variant

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