bace2[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:: COL18A1-AS2; RCAN1; C21orf91-OT1; KRTAP13-2; KRTAP19-9P; VN2R20P; CYCSP42; HSPA13; RNU6-772P; BACH1-IT2; KRTAP25-1; RPL10P1; HSPD1P7; LOC107985515; LINC01683; KRTAP10-11; HLCS; LOC107985475; COL6A2; LOC107985512; SNRPGP13; LINC01548; MCM3AP-AS1; KRTAP13-1; CYCSP41; LCA5L; DIP2A; LOC105372829; PCNT; KRT18P2; RPS3AP1; C21orf62-AS1; LOC105372826; TFF1; BAGE2; LOC102724800; SNX18P11; ATP5PF; JCADP1; BACH1-IT3; RNA18SN1; TIAM1; LINC01424; LINC01673; SIM2; VN1R8P; FTCD; LOC105379507; C2CD2; ATP5PO; ITSN1; LOC105372740; RPS26P1; MIR155; LOC107985492; LOC105372766; B3GALT5-AS1; LINC00323; NF1P3; TSPEAR; LINC02940; KRTAP8-1; LOC110091776; KRTAP20-3; LINC00160; LINC01426; SH3BGR; ADAMTS1; SLC19A1; RPL3P1; LOC105369305; LLPHP2; SRSF9P1; PAXBP1; B3GALT5; LINC00313; RPL18AP2; LOC105369308; CFAP298; BRWD1-AS1; LINC03039; ZNF114P1; CBR3-AS1; LOC105372760; COL18A1-AS1; LOC105377134; ADARB1; KRTAP19-1; CBR3; GAPDHP16; ZNF299P; KRTAP10-8; KRTAP13-6P; CYYR1; RBMX2P1; KRTAP22-1; C21orf62; DPRXP5; CYP4F29P; ERLEC1P1; LOC105372814; MIR6130; RNU6-113P; MIR6724-1; SOD1; RRP1; TMPRSS15; ETS2-AS1; LOC105369302; MIR10396A; PKNOX1; MIR4759; RBPMSLP; YRDCP3; MSANTD2P1; C1QBPP1; LOC101930100; CHODL-AS1; TEKT4P2; KRTAP10-4; LOC102723380; RNA28SN3; RNU6-1149P; LINC01695; SAMSN1-AS1; KRTAP10-7; VPS26C; ANKRD20A18P; KRTAP10-10; MYL6P2; LOC105372757; KRTAP20-2; LINC01668; OLIG1; LOC105369299; LOC107985486; SNX18P10; FDX1P2; ZNF295-AS1; GRIK1-AS1; LOC107985483; KRTAP27-1; CDC27P11; RUNX1-IT1; LINC00163; TERF1P1; LOC101928368; ASMER1; MTRES1P2; CRYAA; RSPH1-DT; PRMT2; LINC01690; POLR2CP1; LTN1; USP16; LOC105372777; LOC105372817; LINC01692; RNA5SP490; LOC105372774; VDAC2P1; CYYR1-AS1; PIGP; C21orf58; PSMD4P1; KRTAP19-6; IL10RB-DT; LINC01694; POFUT2; CDRT15P9; RIPK4; GABPA; LOC105372734; LOC101927615; LOC105372791; NIPA2P3; BTG3-AS1; LINC00158; PCP4; COL6A1; LOC107985500; PSMA6P3; MCM3AP; KRTAP24-1; LOC105372797; DNMT3L; MIR125B2; DSCR9; KCNE1; EIF4A1P1; RNU6-1326P; GTF2IP2; ANKRD20A16P; LOC105372768; RNA28SN2; RNA45SN2; RNA45SN3; AATBC; RIPPLY3; FRGCA; CHODL; NCSTNP1; MIS18A; MIR99A; H2AZP1; CNN2P7; IFNAR2; RPL34P3; LINC01425; PCSEAT; KRTAP19-3; NRIP1; TPTE; TSPEAR-AS2; LINC00112; MAPK6P2; LOC105372745; RNU6-992P; MTCO1P3; C21orf91; LOC105377139; GRIK1-AS2; KRTAP10-13P; MIR4760; RNU1-98P; MX2; SREK1IP1P1; SSR4P1; RPS9P1; ZNF355P; LRRC3; GRIK1; FEM1AP1; RNU6-696P; KRTAP13-5P; ITGB2-AS1; KRTAP6-2; MTCYBP21; SNORA80A; LOC107985480; USP25; KRTAP12-3; KRTAP21-3; KRTAP12-5P; LOC105377136; LINC00316; LINC01684; OR4K11P; FGF7P2; IGSF5; PWP2; LOC101928107; LINC00945; KRTAP8-3P; UMODL1-AS1; ATP5MFP1; LINC00317; C21orf140; KRTAP10-5; ERVH48-1; FRG2MP; CCT8; ERG; LOC105369304; ANKRD30BP1; LOC107985474; GET1; DSCAM; LINC01679; IGHV1OR21-1; SUMO3; LIPI; KRTAP10-1; LINC01667; LOC102725065; LINC01671; LOC107985494; LINC01549; JAM2; KRTAP10-6; RN7SKP236; SNORD159; SNX18P13; PPIAP1; LOC107987300; LOC105372762; KRTAP21-2; PCBP3-AS1; TFF3; LOC107987303; LOC105372825; KCNJ6-AS1; MRAP-AS1; LOC105372759; CYP2C63P; MORC3; LOC107985511; SLC37A1; LOC105372842; MYL6P1; RPSAP64; COL18A1; SNORA91; RNU1-139P; LOC107985488; VN1R109P; KRTAP26-1; BACE2; AIRE; TTC3-AS1; MTCO1P1; RNA28SN1; RNA5SP492; AGPAT3; MIR3156-3; LOC105372802; MIR5692B; DSCR8; TMPRSS2; LOC110467529; RN7SL163P; CFAP298-TCP10L; UBE3AP2; LINC00308; LINC01689; LINC00114; LOC105372750; MIR6508; KRTAP19-11P; KRTAP7-1; CBR1; SLC5A3; KRTAP15-1; MAP3K7CL; TMEM97P1; DNMT3L-AS1; MTND2P1; RUNX1; HSF2BP; RNU4-45P; FAM3B; CLDN14-AS1; TRG-GCC1-5; PCBP2P1; FDPSP6; TPT1P1; LOC101928078; CFAP410; LOC105372813; MIR3648-2; MIR6815; RPL39P40; MIR802; RPL12P9; LOC105372793; SETD4-AS1; RAD23BP3; CBR1-AS1; LOC105379514; PICSAR; LINC00159; LINC02575; IFNGR2; RIMKLBP1; RNA5-8SP10; LOC105372770; EEF1A1P1; CXADR; GET1-SH3BGR; UMODL1; ITGB2; CXADRP1; HUNK; PSMG1; MIR99AHG; BNAT1; ANKRD30BP2; GATD3; KCNJ15; RNU6-954P; RNA5-8SN3; PPIAP22; PDE9A-AS1; KRTAP20-1; BRWD1-AS2; KRTAP12-1; LINC00205; LOC102724355; KRTAP19-8; URB1; RPS26P4; SPATA20P1; PDE9A; LOC112268283; LOC105372756; LOC105372776; BRWD1; LOC107985485; NEK4P1; RNU6-614P; LOC105372733; LOC105372753; PAXBP1-AS1; LOC107985508; LOC100420035; LOC101927345; SNORD74B; UBASH3A; NDUFV3; LSS; LOC105372839; SLX9; LOC105372773; LINC01666; LOC105372836; WDR4; FAM207CP; RN7SL52P; EXOSC3P1; KRTAP19-10P; MIR548X; LINC00319; RNA5-8SN2; KRTAP19-5; LOC107985482; KRTAP19-2; RHOT1P2; RNA5SP489; RNA45SN1; MIR6070; LINC01697; MIR3648-1; SCAF4; KRTAP20-4; LOC102723668; LOC101928255; KRTAP10-2; LOC105372747; LOC107985502; UBE2G2; MIR3197; APP; LINC01687; LINC00113; LOC105372804; LINC00479; SYNJ1; RPL8P2; LOC105369292; PPP6R2P1; MX1; S100B; U2AF1; LOC105372790; VN1R7P; SOD1-DT; ICOSLG; D21S2088E; OLIG2; RPL37P4; LOC105372767; LOC107985516; RPL23AP12; SMIM11; CLDN17; LOC105372787; TFF2; NCOR1P4; MRPS6; MIR10396B; KRTAP10-3; IFNAR1; KCNE2; MEMO1P1; LOC101928212; ABCC13; HMGN1P2; NCAM2; MIR6724-3; SPATC1L; LOC107985499; RRP1B; CRYZL1; KRTAP10-12; RNU6-396P; RNU6-926P; LINC01678; OR7E23P; CBS; POTED; KRTAP12-2; MRPL39; CDRT15P8; RPS20P1; LINC01547; LINC00334; RPS26P5; TTC3; LOC101928796; TMPRSS3; METTL21AP1; RPL23AP3; LOC105379505; RPS5P2; RPS5P3; CSTB; IMMTP1; LINC01423; KRTAP23-1; CLDN8; RN7SL740P; MIR548XHG; OR4K12P; THUMPD1P1; LOC101928398; RPL23P2; RNA18SP5; DSCAM-AS1; TRPM2-AS; LOC100419737; KRTAP21-4P; KRTAP11-1; KCNJ6; KRTAP8-2P; DSCR4; RNU6-859P; PDXK; GRAMD4P1; RNU6-286P; KRTAP10-9; RNU6-123P; LOC101928126; KRTAP6-1; LINC01674; MIRLET7C; LINC00515; KRTAP13-3; USF1P1; LOC100506403; MRAP; KRTAP21-1; LOC107987299; SON; DSTNP1; LOC107985513; LOC101927745; LONRF2P5; LINC01700; DONSON; LOC105372801; DSCAM-IT1; LINC00322; LOC101928269; SOWAHCP2; RNU6-426P; RNU6-1150P; CDC27P9; MIR4327; RN7SKP147; RNU2-55P; LOC105372824; GPX1P2; SMIM34; ETS2; DSCR10; PPP1R2P2; RNA5-8SN1; CDC27P10; MIR6501; KRTAP22-2; TIMM9P2; RNA5SP488; LOC107985490; LOC105372821; LOC100419041; PCBP3; DOP1B; LINC00310; SAMSN1; MIR8069; LOC105372775; H2BC12L; LOC101928369; LINC00314; YBEY; LINC00320; SLC6A6P1; TRAPPC10; KRTAP13-4; LOC105372758; RNA5SP491; LOC105372798; TSPEAR-AS1; LOC105369306; MIR6724-4; LOC654338; TUBAP1; SNX19P1; TRPM2; MIR155HG; MIR3118-1; LOC105372789; LOC105372772; LOC107985478; BTF3L4P1; EIF3FP1; RBM11; RNA18SN2; LOC105372749; RWDD2B; ZBTB21; LOC105372738; ASNSP2; RPL31P1; KRTAP19-7; LOC100288590; CHAF1B; LRRC3-DT; LINC02573; N6AMT1; DNAJC28; CLDN14; RSPH1; SETD4; LINC00189; GAPDHP14; ANKRD20A11P; LINC00649; FTCD-AS1; GART; LINC00307; ADAMTS5; DIP2A-IT1; LINC00111; FBXW11P1; LOC105372841; TCP10L; RNA18SN3; MTND6P21; MIR6814; RN7SL678P; CLIC6; PLAC4; MRPL20P1; MTND5P1; SIK1; LOC105369294; LINC00161; MRPL51P2; KRTAP6-3; KRTAP19-4; EVA1C; PRDM15; DYRK1A; RPL37P3; LOC107985504; LOC105372812; LOC102723475; LINC02943; EZH2P1; BTF3P6; BACH1; BTG3; IL10RB; KRTAP12-4; RPL13AP7; HMGN1; MTCO3P26; RNF6P1; MIR6724-2; LINC01436; LOC105372809; TMEM50B; RNGTTP1; PTTG1IP; SLC25A15P4; URB1-AS1; ABCG1; GXYLT1P2; TIAM1-AS1; LOC105372815; MARCKSP1; PFKL; See more...

Location information:

Clinical significance:

ID:: 48486531

variant

2.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: MTND5P1; RPL37P3; PRDM15; PLAC4; C21orf62-AS1; MIR6814; DYRK1A; ITSN1; LINC00649; SETD4; LRRC3-DT; MTND6P21; LOC105372829; MRPL20P1; LINC00161; TCP10L; CLDN14; LINC00111; TRPM2; LOC105369294; KRTAP19-4; DNAJC28; FTCD-AS1; RPL31P1; LOC105372766; LINC00307; LOC105372789; LOC105372809; RNGTTP1; PTTG1IP; URB1-AS1; RNF6P1; BTG3; HSPD1P7; LINC02573; ATP5PF; GAPDHP14; TMEM50B; LINC00189; LOC100288590; IL10RB; LINC01683; ADAMTS5; CHAF1B; SNRPGP13; DIP2A-IT1; LOC105372812; LINC03039; LOC107985478; SIK1; MCM3AP-AS1; LINC01436; LOC105372815; EZH2P1; RBM11; RPL13AP7; LOC105372749; PFKL; KRTAP6-3; VN2R20P; COL6A2; HMGN1; MARCKSP1; LOC105372772; LOC107985504; KRTAP12-4; MRPL51P2; KRTAP19-3; TIAM1-AS1; EVA1C; MAPK6P2; BTF3P6; LINC01425; ABCG1; LOC105372745; C21orf91; DNMT3L; LINC00112; RNU1-98P; MORC3; LOC105372768; RNU6-1326P; MIR99A; RPS9P1; TSPEAR-AS2; DSCR8; MIR4760; IFNAR2; LOC107985474; LINC01679; LINC00158; PSMA6P3; UMODL1-AS1; SSR4P1; LOC107985494; NRIP1; MIS18A; RIPPLY3; PCSEAT; MX2; CHODL; COL6A1; MIR125B2; ITGB2-AS1; DSCR9; NCSTNP1; LOC107985500; AATBC; LINC00316; KRTAP15-1; H2AZP1; BACE2; KRTAP19-11P; BTG3-AS1; FRGCA; TFF3; SREK1IP1P1; NIPA2P3; USP25; RPL34P3; LINC01671; RNU6-696P; PCP4; MCM3AP; RNU6-992P; LOC105377139; KRTAP24-1; LOC105377136; SNORA80A; MTCYBP21; LOC105372791; KRTAP10-13P; KRTAP12-3; LOC107985480; KRTAP13-5P; CBR1; GRIK1; KRTAP12-5P; KRTAP6-2; LTN1; LINC01690; KCNE1; MYL6P2; GRIK1-AS2; SOD1; USP16; KRTAP19-6; MTCO1P3; RSPH1-DT; ASMER1; KRTAP10-7; KRTAP20-2; KRTAP10-10; TMPRSS15; KRTAP10-4; RUNX1-IT1; SAMSN1-AS1; LOC105369299; MSANTD2P1; OLIG1; LOC105372814; RNU6-1149P; ETS2-AS1; LOC105369302; VPS26C; LINC01695; MTRES1P2; LINC01692; EIF4A1P1; CHODL-AS1; PRMT2; MIR6130; RNA5SP490; PKNOX1; ZNF299P; LINC01684; PIGP; GABPA; DPRXP5; RBPMSLP; LOC107985483; C1QBPP1; PSMD4P1; LRRC3; POFUT2; LOC107985486; YRDCP3; LOC105372817; KRTAP21-3; LINC01694; CYYR1-AS1; LOC105372757; LOC105372777; IL10RB-DT; FDX1P2; POLR2CP1; C21orf58; LOC105372774; LOC105372797; VDAC2P1; KRTAP19-5; LOC101928368; GRIK1-AS1; PPIAP22; SETD4-AS1; GET1-SH3BGR; UMODL1; KCNJ15; MIR6815; LOC102724355; EXOSC3P1; PSMG1; KRTAP12-1; NDUFV3; HUNK; CXADR; ITGB2; NEK4P1; KRTAP20-4; TTC3; IFNGR2; KRTAP19-8; LSS; RPS26P4; LINC01687; HSF2BP; SPATA20P1; RPL39P40; RUNX1; UBASH3A; FDPSP6; TRG-GCC1-5; LOC101928078; CFAP410; DNMT3L-AS1; LINC02575; TPT1P1; MTND2P1; KRTAP20-1; CBR1-AS1; RPL23P2; PCBP2P1; PICSAR; FAM3B; LINC01689; LOC107985502; BRWD1; LOC105372773; RIMKLBP1; LOC105372790; LOC105372836; WDR4; SNORD74B; LOC105372750; GATD3; DSCAM-IT1; RNU4-45P; LOC105372770; RAD23BP3; LOC105372753; RPL12P9; MIR6070; EEF1A1P1; LOC105372813; LOC100420035; RPL8P2; BRWD1-AS2; LOC105372793; LOC107985485; KRTAP19-2; LINC00479; LINC01697; MIR99AHG; LOC105372762; LOC105372776; PDE9A-AS1; KRTAP26-1; TMPRSS2; SCAF4; LOC105372759; SLX9; URB1; MRAP-AS1; LOC107985511; LOC107987300; LOC105372802; AIRE; PPIAP1; LOC105372825; MYL6P1; ERG; CYP2C63P; LOC107985508; KRTAP21-2; AGPAT3; LINC00159; LOC107985488; SNORA91; LINC01549; PCBP3-AS1; CCT8; RNU1-139P; LIPI; LOC107987303; SUMO3; JAM2; KRTAP10-1; KRTAP10-6; SNORD159; RN7SKP236; KRTAP8-3P; C21orf140; ATP5MFP1; ERVH48-1; LINC00114; PWP2; GET1; BNAT1; IGSF5; SLC37A1; KRTAP7-1; RNA5SP492; TMEM97P1; LINC00308; LINC00945; LOC102725065; DSCAM; PDE9A; LOC105372839; LINC00317; LINC00205; LOC105372756; RNA5SP489; KRTAP10-5; LOC101928107; KCNJ6-AS1; CFAP298-TCP10L; LOC105369304; LOC105372801; LOC101928269; CLDN14-AS1; BTF3L4P1; RNU6-426P; TTC3-AS1; RN7SKP147; MIR802; RN7SL163P; SLC5A3; COL18A1; UBE3AP2; MIR4327; KRTAP13-4; RNU6-1150P; LOC105372842; MAP3K7CL; MIR6508; LOC107987299; KRTAP10-9; MIR5692B; MIR155HG; KRTAP19-7; ZBTB21; LINC00322; PAXBP1-AS1; GPX1P2; LOC105372738; USF1P1; LOC100506403; LINC00310; RPSAP64; DONSON; LINC01700; SAMSN1; LOC105372758; LOC101927745; SMIM34; LINC00314; YBEY; KRTAP21-1; ETS2; RSPH1; TRAPPC10; BACH1; TSPEAR-AS1; KRTAP22-2; LOC105369306; LOC101928369; LINC00320; LOC107985490; LOC105372798; LOC105372821; THUMPD1P1; SON; LOC105372775; FBXW11P1; KRTAP8-2P; PDXK; CLIC6; PPP1R2P2; RN7SL678P; CSTB; LOC105372824; RPS5P2; PCBP3; N6AMT1; RNU2-55P; LOC101928796; DSCR10; LINC00113; RNU6-396P; LOC105372841; D21S2088E; MIR548XHG; MRAP; KRTAP13-3; DSCR4; TRPM2-AS; RWDD2B; TFF2; LOC105372804; LOC105369292; TUBAP1; SMIM11; RPL37P4; DOP1B; RNU6-859P; UBE2G2; CRYZL1; RPS20P1; RNA5SP491; SLC6A6P1; LINC02943; LINC01423; LOC105372747; CLDN17; KRTAP10-2; SYNJ1; APP; CLDN8; KCNE2; LINC01547; RRP1B; MIR3197; LOC101928398; MEMO1P1; ICOSLG; KRTAP23-1; SPATC1L; SOD1-DT; ABCC13; MIR548X; MIRLET7C; LINC00334; S100B; TIMM9P2; LOC101928212; LINC00319; LOC105372767; MRPS6; RPS26P5; KRTAP10-3; IFNAR1; KCNJ6; LOC107985513; LOC107985499; IMMTP1; MRPL39; H2BC12L; NCAM2; RN7SL740P; KRTAP12-2; RPL23AP12; RPS5P3; METTL21AP1; LOC100419737; LOC101928255; GART; OR7E23P; U2AF1; LINC00515; KRTAP6-1; KRTAP10-12; LINC01678; LOC107985516; LOC105372787; MIR6501; DSTNP1; LOC105372760; MX1; RNU6-123P; KRTAP25-1; CBS; HMGN1P2; LOC105372740; TSPEAR; SRSF9P1; ATP5PO; LOC102724800; LINC00313; KRTAP19-10P; RPS26P1; LINC01668; LOC101928126; CRYAA; LOC107985512; LOC107985515; PAXBP1; KRT18P2; RNU6-772P; RPS3AP1; KRTAP22-1; B3GALT5-AS1; HLCS; TIAM1; TMPRSS3; LOC102723380; LINC01673; MIR155; LOC107985492; RNU6-926P; RCAN1; RRP1; DIP2A; DSCAM-AS1; KRTAP21-4P; OLIG2; B3GALT5; LCA5L; C21orf91-OT1; KRTAP13-2; COL18A1-AS2; KRTAP20-3; CYCSP42; MIR4759; KRTAP11-1; TFF1; RNU6-113P; KRTAP19-9P; PCNT; ADARB1; LOC105369305; HSPA13; COL18A1-AS1; C21orf62; BACH1-IT2; ADAMTS1; LINC01426; LOC105369308; SLC19A1; RPL18AP2; KRTAP8-1; RIPK4; RPL3P1; RPL23AP3; SIM2; LLPHP2; KRTAP19-1; GAPDHP16; BACH1-IT3; LINC00160; KRTAP27-1; CYYR1; KRTAP13-6P; SH3BGR; RBMX2P1; CFAP298; LINC00163; BRWD1-AS1; LOC105372826; ZNF295-AS1; JCADP1; RPL10P1; C2CD2; CBR3-AS1; LINC01424; LINC00323; FTCD; LINC02940; KRTAP10-8; KRTAP13-1; LINC01548; KRTAP10-11; CBR3; See more...

Location information:

Clinical significance:

ID:: 48468778

variant

3.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: KRTAP10-12; LINC01678; BRWD1-AS2; RPS26P4; LINC00479; PDE9A-AS1; LOC105372836; WDR4; HSF2BP; LOC105372813; DNMT3L-AS1; GATD3; LOC107985502; PCBP2P1; CBR1-AS1; DSCAM-IT1; TTC3; LINC01547; SLX9; UBASH3A; LOC107985499; NDUFV3; MTND2P1; LINC02575; RIMKLBP1; MIR6815; KCNJ15; SPATA20P1; PICSAR; SETD4-AS1; RSPH1-DT; KRTAP12-1; GET1-SH3BGR; ITGB2; LOC101928368; PSMG1; RUNX1; CFAP410; U2AF1; LOC105372817; PRMT2; PKNOX1; KRTAP10-13P; LOC105372797; LOC105372814; LOC107985480; DSCR9; LINC00316; PSMD4P1; DPRXP5; PIGP; YRDCP3; LRRC3; POFUT2; KRTAP10-4; KRTAP10-10; MTCO1P3; MYL6P2; RNU6-1149P; RUNX1-IT1; VPS26C; KRTAP12-5P; MTCYBP21; RNU6-992P; LOC105377139; DSCR8; BACE2; MYL6P1; MX2; KRTAP10-5; KRTAP12-3; LOC107985500; ITGB2-AS1; RNU6-696P; PCSEAT; RIPPLY3; FRGCA; CBR1; MCM3AP; LINC01671; LINC01679; H2AZP1; PCP4; UMODL1-AS1; DNMT3L; IGSF5; ERG; COL6A1; PSMA6P3; TFF3; TSPEAR-AS2; AATBC; LOC107987303; AGPAT3; ATP5MFP1; MIR4760; LINC00112; SSR4P1; MORC3; RPL34P3; RPS9P1; CBR3; BRWD1-AS1; LOC105372825; PRDM15; ABCG1; RPL18AP2; DIP2A-IT1; MRPL51P2; LOC107985478; SIM2; LINC01436; LINC03039; KRTAP12-4; RNF6P1; ADARB1; EZH2P1; COL6A2; TRPM2; LOC105372809; MCM3AP-AS1; LOC100288590; FTCD-AS1; LINC00323; LOC105372812; LOC105372829; RPS26P1; SETD4; CLDN14; SNRPGP13; LINC02940; PTTG1IP; LINC00111; LINC01424; SRSF9P1; DYRK1A; LOC105369294; RPL31P1; PLAC4; MRPL20P1; RIPK4; CRYAA; CBR3-AS1; TSPEAR; JCADP1; LOC105369308; SH3BGR; B3GALT5; FTCD; LINC01694; RPL3P1; SLC19A1; KRTAP10-8; LOC105369305; C21orf58; LOC102723380; COL18A1-AS2; COL18A1-AS1; RRP1; KRTAP10-11; LINC00313; ZNF295-AS1; HLCS; C2CD2; TFF1; KRTAP10-7; LOC107985492; DIP2A; LINC00163; LOC105372826; RNU6-859P; LCA5L; LOC102724800; ETS2-AS1; LINC01668; TSPEAR-AS1; RPL23AP3; B3GALT5-AS1; PCNT; LOC101928796; DSCR4; KCNJ6; TIMM9P2; LOC105369306; ICOSLG; LOC101928255; KRTAP12-2; LOC101928212; DSCAM-AS1; TMPRSS3; RPL23AP12; H2BC12L; MX1; RPS20P1; SPATC1L; LINC00334; LOC105372801; RNU6-396P; CBS; MIR3197; DSCR10; KRTAP10-3; MEMO1P1; LINC01423; RRP1B; METTL21AP1; KRTAP10-2; LOC107985513; LOC105372841; S100B; TRPM2-AS; TFF2; LOC101928398; IMMTP1; LINC00319; LOC105372821; DOP1B; RN7SL678P; SIK1; RNA5SP491; LINC01700; LINC02943; RNU6-1150P; LOC105372804; PCBP3; UBE2G2; LOC105372824; PFKL; LOC105372815; LOC101928369; TRAPPC10; CSTB; PDXK; CHAF1B; KRTAP10-9; LRRC3-DT; LOC105372798; LINC00322; HMGN1; ZBTB21; ETS2; MTND6P21; MIR6814; LOC100506403; PPP1R2P2; YBEY; LOC101928269; MTND5P1; LOC107985504; RSPH1; LOC107987299; RPSAP64; MIR6508; MIR5692B; COL18A1; KCNJ6-AS1; TTC3-AS1; LOC105372842; MIR802; LSS; LINC00205; TMEM97P1; MIR6070; BNAT1; SUMO3; ERVH48-1; LOC105372839; SNORD159; GET1; KRTAP10-6; LINC00114; PWP2; LOC102725065; KRTAP10-1; CLDN14-AS1; LOC105372802; PCBP3-AS1; SNORA91; PDE9A; TMPRSS2; SLC37A1; RNA5SP492; LOC107985485; AIRE; BRWD1; DSCAM; FAM3B; LOC107987300; UMODL1; See more...

Location information:

Clinical significance:

ID:: 48476460

variant

4.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: AIRE; LSS; PSMG1; SNORA91; KCNJ6-AS1; KRTAP12-1; UMODL1; GET1-SH3BGR; MIR6070; MIR6815; NDUFV3; PDE9A-AS1; LOC105372839; LOC107985485; LINC00479; GET1; SLX9; MIR6508; PDE9A; BNAT1; LINC00205; BRWD1; LOC102725065; FAM3B; LOC105372836; LINC00114; GATD3; PICSAR; UBASH3A; DYRK1A; SPATA20P1; MRPL20P1; KRTAP10-6; PCBP2P1; PTTG1IP; MTND5P1; RSPH1; PRDM15; MIR6814; MTND6P21; LOC101928369; SIK1; ABCG1; LINC02943; LOC105369294; HMGN1; RN7SL678P; LOC105372815; LOC107985504; PFKL; MRPL51P2; LOC105372812; LRRC3-DT; CLDN14; TRPM2; LOC107985513; LOC107987299; CSTB; LOC105372824; TRPM2-AS; ZBTB21; LOC105372801; LINC01700; ETS2; RNU6-396P; DSCR10; LOC105372804; H2BC12L; RNU6-1150P; YBEY; TRAPPC10; LOC105372841; RNA5SP491; TMPRSS3; DSCAM-AS1; DSTNP1; PCBP3; LOC105372798; TSPEAR-AS1; LOC105372821; KCNJ6; KRTAP10-2; TIMM9P2; LOC101928212; TFF2; LINC00322; PDXK; KRTAP10-9; RRP1B; KRTAP10-10; LOC101928398; KRTAP10-4; LINC00163; LINC00313; ZNF295-AS1; LOC107985492; LINC01668; CRYAA; LINC01694; C21orf58; RIPK4; LOC105372797; LOC105372817; PIGP; B3GALT5; KRTAP10-11; RRP1; VPS26C; LCA5L; LOC105369305; COL18A1-AS1; KRTAP10-7; ETS2-AS1; C2CD2; LOC102723380; PLAC4; LOC105372826; FTCD-AS1; LINC02940; JCADP1; DIP2A-IT1; LINC03039; BRWD1-AS1; SH3BGR; TSPEAR; LOC102724800; LINC01424; KRTAP12-4; LOC105369308; RPL18AP2; ADARB1; LOC107985478; SIM2; KRTAP10-8; SNRPGP13; RNF6P1; COL6A2; LOC105372809; LOC105372829; DIP2A; LOC100288590; LINC00111; TFF1; SLC19A1; COL18A1-AS2; PCNT; B3GALT5-AS1; PCBP3-AS1; FTCD; LINC00323; LOC105372825; AGPAT3; LOC107987300; MCM3AP-AS1; HLCS; RPL31P1; LOC105372842; MTCYBP21; COL18A1; TMPRSS2; MIR5692B; RPSAP64; SSR4P1; TTC3-AS1; MYL6P1; FRGCA; SLC37A1; RNA5SP492; TMEM97P1; KRTAP12-5P; LOC105372802; DNMT3L; BACE2; DSCAM; DSCR8; TSPEAR-AS2; MX2; KRTAP10-5; SUMO3; ITGB2-AS1; LINC01671; KRTAP10-1; LOC107987303; KRTAP12-3; SNORD159; COL6A1; PWP2; ERG; MYL6P2; IGSF5; LINC01679; ERVH48-1; TFF3; PSMA6P3; MIR4760; MTCO1P3; LINC00112; UMODL1-AS1; LOC101928368; LOC107985500; PCSEAT; RNU6-696P; DSCR9; LINC00316; PRMT2; KRTAP10-13P; MCM3AP; RIPPLY3; LRRC3; DPRXP5; LOC105372814; RSPH1-DT; LOC107985480; YRDCP3; POFUT2; LOC105377139; PCP4; RNU6-1149P; H2AZP1; U2AF1; RNU6-859P; UBE2G2; IMMTP1; ITGB2; AATBC; RPS26P4; S100B; PKNOX1; KCNJ15; RPL23AP12; CBS; MX1; METTL21AP1; KRTAP10-12; BRWD1-AS2; LINC01678; KRTAP12-2; LOC105372813; LOC101928255; LINC02575; HSF2BP; LINC00319; DNMT3L-AS1; CFAP410; LINC00334; KRTAP10-3; DSCR4; LOC101928796; LINC01423; DSCAM-IT1; ICOSLG; MIR3197; SPATC1L; LOC107985502; WDR4; LOC107985499; TTC3; LINC01547; See more...

Location information:

Clinical significance:

ID:: 48471526

variant

5.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: MIR6070; KCNJ6-AS1; LOC105372839; LINC00205; SUMO3; BNAT1; PDE9A-AS1; LOC107985485; COL18A1; LSS; GATD3; RNA5SP492; FAM3B; MIR5692B; LOC105372842; LOC105372836; PDE9A; MIR6508; SLX9; UBASH3A; GET1; PICSAR; KRTAP10-6; LOC102725065; BRWD1; GET1-SH3BGR; PCBP2P1; MIR6815; LINC00114; KRTAP12-1; SNORA91; UMODL1; SPATA20P1; AIRE; PSMG1; MRPL51P2; LOC107987300; LOC105372815; LINC02943; SIK1; PFKL; LOC107985504; LOC105372812; LOC101928369; LOC105372798; PRDM15; TRAPPC10; HMGN1; ZBTB21; LRRC3-DT; MIR6814; MTND5P1; MTND6P21; RSPH1; ETS2; DYRK1A; PCBP3; DSTNP1; LOC105372841; H2BC12L; LOC105372801; TSPEAR-AS1; RNU6-396P; DSCAM-AS1; TMPRSS3; LOC105372821; YBEY; LOC101928212; KRTAP10-2; KCNJ6; TIMM9P2; LINC00322; RRP1B; TFF2; MIR3197; LOC101928398; PDXK; KRTAP10-9; CSTB; LOC105372804; LOC107987299; LINC01700; RNU6-1150P; DSCR10; LOC107985513; TRPM2-AS; CRYAA; LOC105372824; LOC105372797; RIPK4; LINC01694; C21orf58; LINC01424; SLC19A1; LOC105372817; COL18A1-AS1; COL18A1-AS2; B3GALT5; ETS2-AS1; C2CD2; KRTAP10-7; RRP1; KRTAP10-11; LCA5L; LINC01668; LOC102723380; PCNT; TFF1; KRTAP10-4; ZNF295-AS1; SH3BGR; KRTAP10-10; LINC00163; KRTAP12-4; LINC03039; TSPEAR; RPL18AP2; BRWD1-AS1; LINC00313; JCADP1; KRTAP10-8; SNRPGP13; DIP2A-IT1; ADARB1; RNF6P1; ABCG1; LOC107985478; COL6A2; LOC105372829; LOC100288590; LOC105372826; DIP2A; LINC00323; PLAC4; TRPM2; LOC105369294; MCM3AP-AS1; RPL31P1; FTCD-AS1; LINC00111; FTCD; LINC02940; B3GALT5-AS1; KRTAP12-5P; DSCR8; LOC105372809; MTCYBP21; SLC37A1; LOC102724800; DSCAM; PTTG1IP; MCM3AP; FRGCA; LINC01671; BACE2; RPSAP64; ITGB2-AS1; MX2; TSPEAR-AS2; AATBC; LOC107987303; UMODL1-AS1; PSMA6P3; PWP2; TMEM97P1; KRTAP12-3; DNMT3L; PCSEAT; IGSF5; LINC01679; ERVH48-1; KRTAP10-5; MYL6P1; LOC101928368; PCBP3-AS1; KRTAP10-1; TFF3; COL6A1; SNORD159; PCP4; ERG; RSPH1-DT; POFUT2; SSR4P1; TMPRSS2; LOC105372802; AGPAT3; KRTAP10-13P; LOC105372814; LINC00112; LRRC3; PKNOX1; PRMT2; LOC105372825; MIR4760; LINC00316; YRDCP3; LOC107985500; H2AZP1; LOC105377139; MYL6P2; LOC107985480; LINC01678; CBS; KRTAP10-12; MX1; RPL23AP12; RPS26P4; LOC101928796; BRWD1-AS2; LOC105372813; KRTAP12-2; LOC101928255; WDR4; METTL21AP1; KRTAP10-3; RNU6-1149P; MTCO1P3; HSF2BP; LINC02575; LINC00319; DNMT3L-AS1; NDUFV3; ICOSLG; ITGB2; IMMTP1; LINC00479; UBE2G2; S100B; RNU6-859P; LOC107985499; U2AF1; CFAP410; KCNJ15; SPATC1L; DSCAM-IT1; LOC107985502; LINC01547; LINC00334; LINC01423; DSCR4; See more...

Location information:

Clinical significance:

ID:: 48472008

variant

6.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: LCA5L; B3GALT5-AS1; DIP2A; FTCD; LINC02940; TFF1; PCNT; LINC01668; LOC105372826; C2CD2; RPL18AP2; ADARB1; COL18A1-AS1; LINC00323; KRTAP10-11; RRP1; COL18A1-AS2; B3GALT5; SH3BGR; JCADP1; BRWD1-AS1; LINC00313; KRTAP10-8; SLC19A1; LINC01424; LOC102724800; UBE2G2; LOC105372804; CSTB; CRYAA; ICOSLG; TSPEAR; LINC00334; U2AF1; S100B; LOC107985513; IMMTP1; TIMM9P2; LINC01547; MIR3197; KRTAP10-2; LOC101928212; LOC101928398; TFF2; LOC101928255; KRTAP10-12; LINC00319; LINC01423; METTL21AP1; LINC01678; KRTAP10-3; DSCAM-AS1; RRP1B; LOC107985499; KCNJ6; DSCR10; SPATC1L; LOC105372824; RNU6-859P; DSTNP1; KRTAP12-2; CBS; DSCAM-IT1; MX1; RNU6-396P; DSCR4; TMPRSS3; LOC101928796; RPL23AP12; TRPM2-AS; ETS2; LINC00322; RNU6-1150P; ZBTB21; LOC107987299; KRTAP10-9; PDXK; PCBP3; H2BC12L; YBEY; LOC105372841; LOC105372821; LINC01700; LOC105372801; TRAPPC10; LOC101928369; TSPEAR-AS1; KRTAP10-6; LINC01679; LOC107987300; SNORD159; SNORA91; LOC107987303; ERVH48-1; GET1; LOC105372825; LOC102725065; UMODL1-AS1; LINC00114; DSCAM; KRTAP10-5; SUMO3; KRTAP10-1; ERG; PWP2; IGSF5; TMEM97P1; AIRE; MIR5692B; DSCR8; LINC00205; COL18A1; MIR6508; LOC105372802; TMPRSS2; LOC105372842; RPSAP64; PCBP3-AS1; MYL6P1; AGPAT3; GET1-SH3BGR; SLC37A1; KCNJ6-AS1; SPATA20P1; RNA5SP492; PSMG1; UBASH3A; PICSAR; BNAT1; LOC105372813; LINC02575; ITGB2; CFAP410; PDE9A; FAM3B; GATD3; UMODL1; LOC105372836; NDUFV3; LINC00479; LOC105372839; MIR6815; LOC107985502; PCBP2P1; SLX9; WDR4; BRWD1-AS2; HSF2BP; DNMT3L-AS1; LSS; RPS26P4; MIR6070; KCNJ15; KRTAP12-1; LINC00163; LOC102723380; RNU6-1149P; KRTAP10-4; ZNF295-AS1; PDE9A-AS1; BRWD1; MYL6P2; KRTAP10-7; YRDCP3; LOC107985485; KRTAP10-10; C21orf58; POFUT2; LRRC3; ETS2-AS1; SSR4P1; LOC105372814; MIR4760; TFF3; LOC105372817; RIPK4; LINC00112; PKNOX1; LOC101928368; PRMT2; LINC01694; PSMA6P3; TSPEAR-AS2; RSPH1-DT; COL6A1; PCP4; LOC107985480; AATBC; LINC00316; FRGCA; MCM3AP; LOC107985500; DNMT3L; ITGB2-AS1; PCSEAT; KRTAP10-13P; MTCO1P3; H2AZP1; BACE2; KRTAP12-3; MX2; LINC01671; PLAC4; LINC00111; PTTG1IP; KRTAP12-5P; LOC105377139; LOC100288590; LOC105369294; MTCYBP21; LOC105372829; RSPH1; FTCD-AS1; LRRC3-DT; LOC105372809; COL6A2; TRPM2; RNF6P1; LOC107985478; LOC105372812; KRTAP12-4; PFKL; LINC03039; ABCG1; LOC105372815; MIR6814; LINC02943; PRDM15; DIP2A-IT1; SIK1; RPL31P1; SNRPGP13; MCM3AP-AS1; MTND5P1; LOC107985504; HMGN1; MRPL51P2; MTND6P21; See more...

Location information:

Clinical significance:

ID:: 48482309

variant

7.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: LOC107985513; LOC101928398; LINC01700; TFF2; LOC105372804; TMPRSS3; SMIM34; LOC107987299; LOC101928269; LINC00310; RNA5SP491; ZBTB21; DSCR10; DSCAM-AS1; SMIM11; LOC105369306; LOC105372801; KCNJ6; CLIC6; LOC105372798; RPL23AP3; LOC101928212; MEMO1P1; TIMM9P2; LOC100506403; PRDM15; RSPH1; SETD4; MRPL20P1; CLDN14; DYRK1A; LOC105369294; ABCG1; ETS2; LINC02943; MIR6814; LOC107985504; RN7SL678P; HMGN1; LOC105372815; LOC105372812; CHAF1B; DOP1B; PPP1R2P2; EZH2P1; LINC00111; TFF1; LINC02940; LOC107985515; HLCS; LINC00323; B3GALT5-AS1; LOC100288590; PLAC4; SIM2; LOC105372809; LOC102724800; LINC00160; RPS26P1; SH3BGR; SRSF9P1; JCADP1; CBR3; RPL3P1; LOC105369308; BRWD1-AS1; SNRPGP13; LINC01436; RNF6P1; LOC107985478; RUNX1-IT1; LOC107985492; LCA5L; LINC01668; ZNF295-AS1; C2CD2; LOC105369305; LOC105372817; B3GALT5; LINC01426; LOC105372797; RIPK4; CBR3-AS1; PIGP; VPS26C; PSMD4P1; RCAN1; ETS2-AS1; LINC00112; RNU6-1149P; RSPH1-DT; MIR4760; KCNE1; RNU6-696P; RPS9P1; MYL6P2; DPRXP5; LOC101928368; YRDCP3; LOC107985480; LOC105372814; PCSEAT; TFF3; LOC105372791; UMODL1-AS1; LOC105372802; MX2; RIPPLY3; RNU6-992P; DSCR8; TMPRSS2; DSCR9; LOC107985500; SLC37A1; CBR1; C21orf140; RPL34P3; RNA5SP492; MORC3; ERG; MIR802; LINC01671; IGSF5; DSCAM; PCP4; TTC3-AS1; RPSAP64; SPATA20P1; LINC00114; RUNX1; CBR1-AS1; UMODL1; UBASH3A; BACE2; ATP5MFP1; PSMG1; KCNJ6-AS1; LINC00479; MTND2P1; BRWD1; PDE9A; MIR6508; PCBP2P1; GET1-SH3BGR; SNORA91; GET1; LOC105372793; LINC01423; TTC3; PDE9A-AS1; DSCR4; CLDN14-AS1; KCNJ15; RPS20P1; MX1; RPS26P4; METTL21AP1; FAM3B; LOC107985502; DSCAM-IT1; WDR4; LOC107985499; RIMKLBP1; KCNE2; SETD4-AS1; MIR3197; RPL23AP12; BRWD1-AS2; LOC105372813; LOC101928255; See more...

Location information:

Clinical significance:

ID:: 48455172

variant

8.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: RNU6-1149P; MYL6P2; RSPH1-DT; KRTAP10-10; KRTAP10-4; POFUT2; MTCO1P3; PKNOX1; KRTAP10-13P; LRRC3; LOC105372817; PRMT2; PCSEAT; YRDCP3; LOC105372814; UMODL1-AS1; DNMT3L; MX2; TSPEAR-AS2; PSMA6P3; LINC01679; TFF3; MIR4760; COL6A1; PCP4; AGPAT3; IGSF5; LINC00112; H2AZP1; SSR4P1; LOC105372825; MYL6P1; MTCYBP21; LOC105377139; KRTAP12-3; LINC00316; FRGCA; KRTAP12-5P; MCM3AP; LINC01671; LOC107985500; KRTAP10-5; AATBC; BACE2; ITGB2-AS1; KRTAP10-6; SNORD159; PWP2; LOC107987303; KRTAP10-1; AIRE; PCBP3-AS1; LOC107987300; TMPRSS2; SNORA91; TMEM97P1; LINC00205; SLC37A1; MIR5692B; MIR6508; RPSAP64; LOC105372839; COL18A1; LOC105372842; LOC107985485; RNA5SP492; MIR6070; LOC102725065; SUMO3; BRWD1; PDE9A; FAM3B; BNAT1; ERVH48-1; GET1; DSCAM; PCBP2P1; PICSAR; LINC01547; HSF2BP; UBASH3A; CFAP410; LINC02575; GET1-SH3BGR; LINC00479; U2AF1; ITGB2; PSMG1; RPS26P4; LSS; KRTAP10-12; BRWD1-AS2; KRTAP12-1; UMODL1; LINC01678; NDUFV3; SLX9; MIR6815; PDE9A-AS1; DSCAM-IT1; LOC105372813; DNMT3L-AS1; LOC105372836; GATD3; MIR3197; ICOSLG; LOC107985499; LOC107985502; RNU6-396P; IMMTP1; LINC00319; LINC00334; LOC105372804; RNU6-1150P; WDR4; S100B; RRP1B; RNU6-859P; LOC101928398; TFF2; METTL21AP1; DSCAM-AS1; UBE2G2; CSTB; TMPRSS3; H2BC12L; RPL23AP12; LOC105372824; CBS; TIMM9P2; LOC101928212; LOC101928796; TRPM2-AS; KRTAP10-3; LOC101928255; KRTAP10-2; MX1; KRTAP12-2; TSPEAR-AS1; DSTNP1; PDXK; RSPH1; ETS2; LINC01700; LOC107987299; MTND5P1; SPATC1L; LINC02943; PCBP3; SIK1; KRTAP10-9; LINC00322; ZBTB21; YBEY; MTND6P21; LOC105372841; LOC107985504; HMGN1; LINC00111; LINC02940; PFKL; LRRC3-DT; LOC105372821; TRAPPC10; LOC105372829; PLAC4; FTCD-AS1; MCM3AP-AS1; LOC101928369; LOC105372815; RPL31P1; MIR6814; TRPM2; LINC00323; PRDM15; LOC105372809; KRTAP12-4; RPL18AP2; LOC105369294; BRWD1-AS1; LINC03039; COL6A2; DIP2A-IT1; MRPL51P2; RNF6P1; LOC107985478; PTTG1IP; ADARB1; LOC105372812; LOC102723380; FTCD; TFF1; ABCG1; KRTAP10-7; B3GALT5-AS1; C2CD2; LINC00163; DIP2A; ETS2-AS1; PCNT; LOC105372826; ZNF295-AS1; LCA5L; C21orf58; LINC01424; LINC01694; TSPEAR; KRTAP10-11; SH3BGR; COL18A1-AS1; B3GALT5; JCADP1; KRTAP10-8; LOC102724800; LINC00313; LINC01668; CRYAA; RIPK4; RRP1; COL18A1-AS2; SLC19A1; See more...

Location information:

Clinical significance:

ID:: 48487269

variant

9.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: C2CD2; TFF1; KRTAP10-7; LOC102723380; COL18A1-AS1; DIP2A; SLC19A1; KRTAP10-11; KRTAP10-8; TSPEAR; COL18A1-AS2; C21orf58; FTCD; LINC01424; RRP1; PCNT; CRYAA; RIPK4; LOC102724800; LOC105372826; LINC01694; LINC01668; ZNF295-AS1; LINC00163; PICSAR; LINC00313; FAM3B; KRTAP10-1; LOC102725065; SNORD159; PWP2; KRTAP10-6; SUMO3; DSCAM; ERVH48-1; GATD3; BNAT1; LOC105372839; LINC00205; MIR6070; LOC107985485; LSS; RNA5SP492; SLC37A1; MIR5692B; LOC105372842; PDE9A; TMPRSS2; COL18A1; SNORA91; UMODL1; AIRE; TMEM97P1; KRTAP12-1; LOC107987300; PCBP3-AS1; COL6A1; PSMA6P3; DNMT3L; PCSEAT; TFF3; AATBC; LINC01679; TSPEAR-AS2; PCP4; H2AZP1; ITGB2-AS1; LOC107987303; MCM3AP; UMODL1-AS1; FRGCA; LINC01671; KRTAP10-5; BACE2; KRTAP12-5P; MX2; KRTAP12-3; LOC105377139; MTCYBP21; MYL6P1; LINC00112; SSR4P1; LOC105372825; AGPAT3; ICOSLG; MIR4760; KRTAP10-9; RRP1B; LINC00334; MIR3197; LINC00319; KRTAP10-2; KRTAP10-3; TFF2; LOC101928255; KRTAP12-2; TSPEAR-AS1; SPATC1L; LOC101928212; DSTNP1; PCBP3; H2BC12L; LOC105372824; MX1; DSCAM-AS1; CBS; RNU6-396P; S100B; LOC101928796; TMPRSS3; TRPM2-AS; IMMTP1; CSTB; CFAP410; RNU6-1150P; UBASH3A; LINC01547; SLX9; LINC02575; HSF2BP; LOC107985502; LINC00479; WDR4; DSCAM-IT1; LOC105372813; LOC105372836; RNU6-859P; DNMT3L-AS1; LINC01678; NDUFV3; KRTAP10-12; LOC105372809; LINC00323; TRPM2; PDE9A-AS1; RPL31P1; MCM3AP-AS1; UBE2G2; LOC105372812; MIR6815; U2AF1; ITGB2; LOC105372829; LINC00111; ABCG1; COL6A2; ADARB1; PTTG1IP; DIP2A-IT1; PRDM15; LOC107985478; LINC03039; KRTAP12-4; PLAC4; LOC105369294; RPL18AP2; PDXK; PFKL; LOC105372815; LINC00322; FTCD-AS1; LOC105372841; LOC101928369; LRRC3-DT; ZBTB21; LOC105372821; SIK1; YBEY; MRPL51P2; TRAPPC10; MIR6814; MTND5P1; RSPH1; LOC107985504; LOC105372814; YRDCP3; LOC107987299; MTND6P21; KRTAP10-13P; POFUT2; PKNOX1; RNU6-1149P; MTCO1P3; RSPH1-DT; LRRC3; LINC00316; PRMT2; LOC105372817; KRTAP10-4; KRTAP10-10; See more...

Location information:

Clinical significance:

ID:: 48467638

variant

10.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: PRMT2; LOC105372814; YRDCP3; LRRC3; POFUT2; MCM3AP; LINC00316; PKNOX1; KRTAP10-13P; H2AZP1; LOC105377139; MTCO1P3; LINC00112; AATBC; RNU6-1149P; RSPH1-DT; RPL23AP4; MRPL51P2; LOC105372815; SIK1; LOC105372812; PFKL; LOC107985504; ABCG1; PTTG1IP; MTND6P21; LOC105369294; MIR6814; TRPM2; LOC101928369; MTND5P1; RSPH1; LRRC3-DT; PRDM15; RPL18AP2; KRTAP12-4; COL18A1-AS2; SLC19A1; LOC107985478; ADARB1; KRTAP10-8; LINC03039; PLAC4; LINC00111; COL6A2; LOC105372826; DIP2A-IT1; LOC102724800; TFF1; FTCD; LINC01424; PCNT; MCM3AP-AS1; RPL31P1; DIP2A; LOC105372829; LINC00323; FTCD-AS1; LOC105372809; LOC105372813; TSPEAR; WDR4; KRTAP10-12; CBS; LOC101928255; KRTAP10-3; DNMT3L-AS1; DSCAM-IT1; LOC107985502; KRTAP12-2; SPATC1L; LINC01678; LINC00319; RNU6-859P; LINC01547; LOC101928796; ICOSLG; LINC00334; IMMTP1; U2AF1; S100B; HSF2BP; CFAP410; ITGB2; LINC02575; TMPRSS3; MIR3197; TRAPPC10; LOC101928212; UBE2G2; MX1; DSTNP1; TSPEAR-AS1; LOC105372841; DSCAM-AS1; RRP1B; PCBP3; YBEY; H2BC12L; TFF2; TRPM2-AS; RNU6-396P; KRTAP10-9; LOC105372824; LOC105372821; LINC00322; KRTAP10-2; LOC107987299; PDXK; ZBTB21; RNU6-1150P; FRGCA; KRTAP10-5; MIR5692B; TMEM97P1; ERVH48-1; SUMO3; KRTAP10-1; MTCYBP21; CSTB; COL6A1; TFF3; COL18A1; KRTAP12-3; LOC105372825; LINC01671; SSR4P1; PSMA6P3; AGPAT3; SNORD159; ITGB2-AS1; TMPRSS2; KRTAP12-5P; TSPEAR-AS2; UMODL1-AS1; DSCAM; PCBP3-AS1; DNMT3L; PWP2; RNA5SP492; MX2; LINC01679; LINC00479; BACE2; MYL6P1; PCSEAT; BNAT1; SLX9; PDE9A; GATD3; LOC102725065; SLC37A1; LOC107987303; LOC105372839; KRTAP10-6; LOC105372842; PICSAR; UBASH3A; PDE9A-AS1; LOC105372836; MIR6070; AIRE; LOC107987300; SNORA91; LSS; LOC107985485; C21orf58; FAM3B; KRTAP12-1; UMODL1; RIPK4; KRTAP10-11; MIR6815; RRP1; LINC00205; NDUFV3; KRTAP10-7; LINC01694; LOC102723380; LINC01668; CRYAA; C2CD2; LINC00163; COL18A1-AS1; LINC00313; ZNF295-AS1; LOC105372817; KRTAP10-4; KRTAP10-10; See more...

Location information:

Clinical significance:

ID:: 48477731

variant

11.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: LOC102723380; TFF1; LOC102724800; PCNT; C2CD2; LINC01668; CRYAA; TSPEAR; LINC00163; ZNF295-AS1; LINC01424; COL18A1-AS1; LINC00313; SLC19A1; C21orf58; KRTAP10-7; LINC01694; RIPK4; DIP2A; RRP1; KRTAP10-11; COL18A1-AS2; UBASH3A; TMPRSS2; SNORD159; KRTAP10-6; LOC107987300; UMODL1; SLC37A1; RNA5SP492; LOC107985485; AIRE; LINC00205; MIR6070; LOC105372842; PDE9A; TMEM97P1; SNORA91; MIR5692B; PCBP3-AS1; LSS; KRTAP12-1; COL18A1; GATD3; SUMO3; KRTAP10-1; LOC105372839; FAM3B; PICSAR; DSCAM; ERVH48-1; SLX9; BNAT1; PWP2; LOC102725065; LOC107987303; LINC00112; LOC105372825; TFF3; SSR4P1; LINC01679; PCSEAT; TSPEAR-AS2; MYL6P1; KRTAP12-5P; KRTAP12-3; MTCYBP21; AGPAT3; ITGB2-AS1; MX2; BACE2; DNMT3L; KRTAP10-5; FRGCA; MCM3AP; LINC01671; PSMA6P3; COL6A1; UMODL1-AS1; AATBC; S100B; IMMTP1; CSTB; LOC105372824; ICOSLG; RNU6-1150P; TSPEAR-AS1; RNU6-396P; TFF2; MIR3197; LOC105372821; LINC00334; PCBP3; TMPRSS3; CBS; MX1; LOC101928796; TRPM2-AS; DSCAM-AS1; H2BC12L; KRTAP12-2; DSTNP1; KRTAP10-3; KRTAP10-2; KRTAP10-9; SPATC1L; LOC101928255; CFAP410; MIR6815; ITGB2; NDUFV3; U2AF1; RRP1B; LOC101928212; UBE2G2; PDE9A-AS1; LINC02575; LINC01678; KRTAP10-12; RNU6-859P; LOC105372836; LOC107985502; DSCAM-IT1; DNMT3L-AS1; WDR4; HSF2BP; LINC00319; RPL31P1; FTCD-AS1; LINC00479; LOC105372813; FTCD; RPL18AP2; LINC01547; PLAC4; LOC105372829; LINC00111; DIP2A-IT1; LOC105372826; ADARB1; PRDM15; PTTG1IP; ABCG1; LOC105369294; MCM3AP-AS1; LINC03039; KRTAP10-8; LOC107985478; KRTAP12-4; LINC00323; COL6A2; LOC107987299; LRRC3-DT; MTND5P1; RSPH1; LOC105372809; MIR6814; MTND6P21; LOC105372812; MRPL51P2; TRPM2; TRAPPC10; LOC107985504; SIK1; LOC101928369; YBEY; ZBTB21; PDXK; LOC105372841; LINC00322; KRTAP10-4; PFKL; H2AZP1; KRTAP10-10; LOC105377139; LOC105372815; RSPH1-DT; LOC105372814; PRMT2; LRRC3; LOC105372817; POFUT2; LINC00316; PKNOX1; RNU6-1149P; KRTAP10-13P; MTCO1P3; YRDCP3; See more...

Location information:

Clinical significance:

ID:: 48474915

variant

12.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: ZBTB21; LOC105372841; TSPEAR-AS1; LOC107987299; RNU6-1150P; LOC101928369; YBEY; PCBP3; H2BC12L; LOC105372821; LINC00322; TRAPPC10; PDXK; KRTAP10-9; PTTG1IP; MTND6P21; MTND5P1; MIR6814; FTCD-AS1; RSPH1; DIP2A-IT1; ABCG1; LOC107985504; PRDM15; PLAC4; LOC105372812; SIK1; KRTAP12-4; LINC03039; LOC107985478; LOC105372815; PFKL; MRPL51P2; LINC00111; MCM3AP-AS1; RPL31P1; LRRC3-DT; COL6A2; TRPM2; LOC105372829; LOC105372809; PCNT; LINC01668; LOC105372826; LINC00313; LOC102724800; ZNF295-AS1; LINC00163; LINC01424; CRYAA; TSPEAR; RPL18AP2; RIPK4; RRP1; ADARB1; KRTAP10-8; KRTAP10-11; COL18A1-AS1; COL18A1-AS2; SLC19A1; DIP2A; TFF1; C2CD2; FTCD; LINC00323; RSPH1-DT; RNU6-1149P; KRTAP10-10; MTCO1P3; KRTAP10-4; LINC01694; C21orf58; LOC105372817; PRMT2; LRRC3; POFUT2; PKNOX1; LOC105372814; KRTAP10-7; LOC102723380; MTCYBP21; SSR4P1; BACE2; LINC00112; KRTAP10-13P; KRTAP12-5P; LOC105377139; LINC00316; MCM3AP; FRGCA; LINC01671; KRTAP12-3; MX2; ITGB2-AS1; TSPEAR-AS2; COL6A1; SNORA91; H2AZP1; TFF3; PSMA6P3; LOC107987300; DNMT3L; PCSEAT; AIRE; COL18A1; LOC105372842; PDE9A; SLC37A1; LOC105372839; LINC00205; AATBC; MIR5692B; PCBP3-AS1; MYL6P1; RNA5SP492; LOC105372825; LOC102725065; TMEM97P1; TMPRSS2; AGPAT3; UMODL1-AS1; SUMO3; SNORD159; KRTAP10-6; MIR6815; LINC01679; LOC107987303; ERVH48-1; PWP2; KRTAP10-5; ITGB2; UMODL1; PDE9A-AS1; NDUFV3; KRTAP12-1; LOC107985485; KRTAP10-1; LSS; DNMT3L-AS1; FAM3B; WDR4; LOC105372836; LOC105372813; GATD3; PICSAR; HSF2BP; LINC02575; SLX9; CFAP410; LINC00479; MIR6070; UBASH3A; U2AF1; RNU6-859P; UBE2G2; IMMTP1; LOC107985502; CSTB; LOC101928796; BNAT1; LOC105372824; TMPRSS3; RNU6-396P; CBS; S100B; KRTAP10-12; MX1; LINC01678; KRTAP12-2; LOC101928255; MIR3197; KRTAP10-3; LINC00319; TFF2; KRTAP10-2; TRPM2-AS; ICOSLG; DSTNP1; LOC101928212; SPATC1L; LINC00334; RRP1B; LINC01547; See more...

Location information:

Clinical significance:

ID:: 48460210

variant

13.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: KCNJ15; SPATA20P1; UMODL1; NDUFV3; GET1-SH3BGR; PSMG1; HSF2BP; UBASH3A; PCBP2P1; BRWD1; DSCAM-IT1; LOC107985502; FAM3B; LOC105372813; LINC00479; WDR4; RPS26P4; BRWD1-AS2; MIR6070; PDE9A-AS1; LOC105369294; LINC00111; LOC105372809; PLAC4; LOC100288590; MIR6814; RPL31P1; SNRPGP13; LOC105372812; RNF6P1; HMGN1; LOC107985478; LOC107985504; MRPL51P2; LOC105372815; ABCG1; PRDM15; LINC03039; SIK1; LOC107987299; ZBTB21; RSPH1; ETS2; PDXK; LINC00322; LOC105372801; LINC02943; LINC01700; LOC105372821; LOC101928369; MYL6P2; RNU6-1149P; ETS2-AS1; LOC105372814; YRDCP3; LOC105372817; PKNOX1; ZNF295-AS1; LINC00313; LINC02940; RSPH1-DT; TFF1; B3GALT5-AS1; C2CD2; LOC102724800; LCA5L; LINC01668; RIPK4; LOC102723380; BRWD1-AS1; LINC00323; JCADP1; SH3BGR; SNORA91; LOC107987300; LOC105372802; CRYAA; B3GALT5; LINC00114; DSCAM; RNA5SP492; SLC37A1; TMPRSS2; PDE9A; ERVH48-1; GET1; ERG; RPSAP64; IGSF5; MIR5692B; MIR6508; LINC01671; BACE2; PCSEAT; UMODL1-AS1; LOC107985500; LINC00112; MIR4760; FRGCA; PCP4; MX2; LINC01679; TFF3; LOC107985513; DSCR8; U2AF1; LOC105372824; LOC105372804; LOC107985480; DSCR10; MIR3197; LINC00319; LOC101928398; TFF2; RRP1B; DSCAM-AS1; LOC101928255; LOC107985499; METTL21AP1; MX1; H2BC12L; DSCR4; TMPRSS3; CBS; LINC01423; RPL23AP12; TIMM9P2; LOC101928212; See more...

Location information:

Clinical significance:

ID:: 50273197

variant

14.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: TRPM2; LRRC3-DT; MIR6814; MTND6P21; MTND5P1; RSPH1; FTCD-AS1; PRDM15; PTTG1IP; LOC107985504; SIK1; MRPL51P2; PFKL; LOC101928369; LOC105372812; ABCG1; LOC105372815; RNU6-1149P; MTCO1P3; H2AZP1; PCSEAT; RSPH1-DT; LINC00112; LOC105377139; KRTAP10-13P; KRTAP12-3; LOC105372814; PRMT2; LRRC3; AATBC; LINC00316; KRTAP10-7; KRTAP10-4; MCM3AP; C2CD2; LOC102723380; KRTAP10-10; LINC01668; CRYAA; POFUT2; LINC00163; ZNF295-AS1; C21orf58; LINC01694; RIPK4; LOC105372817; RRP1; PKNOX1; COL18A1-AS1; PICSAR; UBASH3A; KRTAP10-6; SNORA91; UMODL1; MIR6815; LSS; NDUFV3; AIRE; KRTAP12-1; LOC107985485; MIR6070; PDE9A; LOC105372839; LINC00205; PDE9A-AS1; LINC00479; LOC107985502; FAM3B; SLX9; LOC105372813; LOC105372836; BNAT1; LOC102725065; TSPEAR-AS2; UMODL1-AS1; LOC107987303; GATD3; DNMT3L; TMPRSS2; MX2; COL6A1; KRTAP10-1; PWP2; LOC107987300; SNORD159; LINC01679; MYL6P1; LOC105372842; TFF3; PSMA6P3; SLC37A1; MTCYBP21; AGPAT3; KRTAP12-5P; PCBP3-AS1; MIR5692B; LOC105372825; ERVH48-1; RNA5SP492; COL18A1; SSR4P1; FRGCA; TMEM97P1; LINC01671; TFF2; LINC00322; BACE2; KRTAP10-5; RRP1B; KRTAP10-9; SUMO3; ITGB2-AS1; LOC105372824; TRPM2-AS; RNU6-1150P; YBEY; TRAPPC10; LOC107987299; PDXK; H2BC12L; ZBTB21; KRTAP10-2; PCBP3; TSPEAR-AS1; LOC105372821; HSF2BP; LOC105372841; CSTB; UBE2G2; LINC01547; U2AF1; LINC00319; LOC101928796; RNU6-396P; MIR3197; CFAP410; LINC00334; IMMTP1; KRTAP10-12; CBS; MX1; LINC01678; ITGB2; LINC02575; TMPRSS3; S100B; DNMT3L-AS1; DSTNP1; SPATC1L; ICOSLG; KRTAP10-3; WDR4; RNU6-859P; LOC101928212; KRTAP12-2; LOC105372829; LINC00111; DIP2A; RPL31P1; LOC101928255; MCM3AP-AS1; PLAC4; LOC102724800; TSPEAR; TFF1; LOC105372826; PCNT; LINC00313; SLC19A1; RPL18AP2; COL18A1-AS2; ADARB1; KRTAP10-8; LINC01424; KRTAP10-11; LOC105372809; FTCD; LOC107985478; LINC00323; COL6A2; DIP2A-IT1; LINC03039; KRTAP12-4; See more...

Location information:

Clinical significance:

ID:: 48471404

variant

15.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: RRP1; KRTAP10-11; LINC00323; COL18A1-AS2; LINC00163; LINC00313; ZNF295-AS1; LOC102723380; LINC01668; LOC105372826; CRYAA; TFF1; RIPK4; LOC102724800; ADARB1; C2CD2; LINC01424; TSPEAR; KRTAP10-8; COL18A1-AS1; DSCAM; BNAT1; LOC107987300; SUMO3; ERVH48-1; PWP2; LOC107987303; KRTAP10-6; LOC102725065; KRTAP10-5; KRTAP10-1; MYL6P1; RNA5SP492; MIR5692B; LINC00205; SNORA91; PDE9A; AIRE; SLC37A1; TMPRSS2; AGPAT3; TMEM97P1; LOC105372839; LOC105372825; COL18A1; LINC01671; DNMT3L; UMODL1-AS1; LINC01679; AATBC; PCSEAT; TFF3; LINC00112; TSPEAR-AS2; H2AZP1; SSR4P1; MIR4760; KRTAP10-13P; LOC105377139; MX2; BACE2; KRTAP12-3; MTCYBP21; LINC00316; KRTAP12-5P; FRGCA; ITGB2-AS1; LINC00319; LOC101928255; LOC101928212; RRP1B; LINC00334; U2AF1; KRTAP10-2; ICOSLG; IMMTP1; UBE2G2; LINC01547; CSTB; MIR3197; TFF2; TMPRSS3; RNU6-859P; TRPM2-AS; DSCAM-AS1; LOC105372824; CBS; KRTAP12-2; MX1; KRTAP10-3; LINC01678; H2BC12L; KRTAP10-12; LOC105372813; GATD3; DNMT3L-AS1; ITGB2; FAM3B; MIR6815; CFAP410; HSF2BP; UBASH3A; LINC02575; PICSAR; PDE9A-AS1; KRTAP12-1; UMODL1; SLX9; NDUFV3; MIR6070; LINC00479; LOC105372836; LOC107985502; DSCAM-IT1; LOC107985478; TRPM2; LOC105372812; PLAC4; LOC105369294; LOC105372809; LOC105372829; WDR4; LRRC3-DT; MIR6814; SIK1; LINC00111; PTTG1IP; KRTAP12-4; ABCG1; PRDM15; LINC03039; MTND6P21; MTND5P1; RPL31P1; LOC105372815; LOC107985504; MRPL51P2; PFKL; PDXK; RSPH1; LOC107987299; ZBTB21; LINC00322; KRTAP10-9; LOC101928369; TSPEAR-AS1; RNU6-1150P; YRDCP3; LOC105372821; TRAPPC10; RNU6-1149P; KRTAP10-4; KRTAP10-7; KRTAP10-10; MTCO1P3; LRRC3; LOC105372814; LOC105372817; POFUT2; RSPH1-DT; PKNOX1; See more...

Location information:

Clinical significance:

ID:: 49355376

variant

16.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: LCA5L; C2CD2; B3GALT5-AS1; TFF1; JCADP1; ZNF295-AS1; LOC102724800; B3GALT5; BRWD1-AS1; SH3BGR; RIPK4; LINC01423; MIR3197; TFF2; LOC107985513; LOC105372804; LOC101928398; MX1; DSCR10; METTL21AP1; TMPRSS3; RPL23AP12; TIMM9P2; DSCAM-AS1; DSCR4; KCNJ6; ZBTB21; ETS2; LOC105372801; RN7SL678P; LOC105372798; LINC01700; LINC02943; LOC105372815; ERG; LINC00114; SNORA91; TMPRSS2; LOC105372802; RNA5SP492; KCNJ6-AS1; RPSAP64; MIR6508; GET1; TTC3; DSCAM; TTC3-AS1; PCBP2P1; PSMG1; GET1-SH3BGR; UBASH3A; UMODL1; KCNJ15; BRWD1-AS2; LOC107985502; DSCAM-IT1; SPATA20P1; BRWD1; FAM3B; LOC105372813; LOC107985499; ETS2-AS1; LINC00479; RPS26P4; VPS26C; MYL6P2; LOC101928368; LOC105372797; LOC105372814; YRDCP3; RNU6-1149P; UMODL1-AS1; PCSEAT; DSCR8; PCP4; IGSF5; MX2; BACE2; TFF3; LINC00112; LOC107985500; DSCR9; MIR4760; LOC100288590; DYRK1A; PLAC4; LINC00111; HMGN1; LOC107985480; LINC02940; PRDM15; ABCG1; MIR6814; SNRPGP13; RNF6P1; LOC105372809; LOC105372812; LINC00323; LOC107985478; LOC105369294; See more...

Location information:

Clinical significance:

ID:: 48475984

variant

17.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: LINC01678; CBS; MX1; RNU6-859P; RPS26P4; MIR3197; LINC00319; HSF2BP; LOC107985499; U2AF1; ICOSLG; LOC105372813; LOC101928255; DSCAM-IT1; WDR4; LOC107985502; RSPH1-DT; LINC00112; MYL6P2; H2AZP1; RNU6-1149P; LOC105377139; MIR4760; AATBC; YRDCP3; LOC105372814; PKNOX1; LOC107985500; AGPAT3; SLC37A1; RNA5SP492; MYL6P1; MX2; MIR5692B; TMPRSS2; PCSEAT; LOC105372825; LINC01679; PWP2; DNMT3L; TFF3; PCP4; IGSF5; LINC01671; UMODL1-AS1; ERVH48-1; TMEM97P1; DSCAM; FRGCA; BACE2; SH3BGR; LOC102724800; B3GALT5-AS1; JCADP1; LOC105372826; RPL31P1; PLAC4; TFF1; LOC105372829; LINC00111; LINC00323; LOC107985478; LOC105372809; LINC03039; C2CD2; ZNF295-AS1; CRYAA; LOC102723380; LINC00313; LINC01668; B3GALT5; RIPK4; RRP1; LOC105372824; LOC105372821; LCA5L; LOC105372817; ZBTB21; LOC107987299; H2BC12L; TRAPPC10; LOC101928212; TMPRSS3; PDXK; TFF2; RRP1B; CSTB; LINC00322; DSCAM-AS1; RNU6-1150P; SIK1; LOC105369294; LOC101928369; MIR6814; ABCG1; PRDM15; RSPH1; LOC105372812; MRPL51P2; LOC105372815; LINC00479; PDE9A-AS1; MIR6508; MIR6070; SNORA91; UBASH3A; GET1-SH3BGR; LOC102725065; LOC107985504; LOC107987300; GATD3; GET1; PDE9A; NDUFV3; UMODL1; FAM3B; See more...

Location information:

Clinical significance:

ID:: 48482310

variant

18.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: RIPK4; B3GALT5; LOC105372797; ZNF295-AS1; LCA5L; C2CD2; ETS2-AS1; BRWD1; LINC00479; MIR6508; PSMG1; UMODL1; GET1-SH3BGR; KCNJ6-AS1; SPATA20P1; GET1; PCBP2P1; FAM3B; LINC00114; SNORA91; BACE2; LOC105372802; TMPRSS2; RPSAP64; MX2; DSCR8; PCSEAT; DSCAM; IGSF5; UMODL1-AS1; DSCAM-AS1; ERG; PCP4; KCNJ6; LINC01700; DSCR10; ZBTB21; LOC105372801; LOC105372804; LOC107985513; LOC101928398; TIMM9P2; DSCAM-IT1; LOC107985502; BRWD1-AS2; RPS26P4; KCNJ15; METTL21AP1; DSCR4; RPL23AP12; MX1; LOC105372813; MIR3197; LINC01423; LOC107985499; RNF6P1; BRWD1-AS1; JCADP1; LINC02940; PLAC4; LOC105369294; LINC00111; LOC102724800; ABCG1; LINC00323; SH3BGR; LOC105372809; LOC100288590; LINC02943; B3GALT5-AS1; LOC107985478; MIR6814; PRDM15; ETS2; SNRPGP13; LOC105372798; HMGN1; DYRK1A; LOC105372812; LOC101928368; LOC107985480; MIR4760; LINC00112; MYL6P2; YRDCP3; LOC107985500; See more...

Location information:

Clinical significance:

ID:: 48466598

variant

19.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: MIR4760; LINC00112; MYL6P2; RSPH1-DT; MX2; LOC105372814; PCP4; LOC107985500; PCSEAT; LOC105372804; METTL21AP1; DSCAM-IT1; RPL23AP12; MX1; LOC101928212; LOC107985499; LOC101928255; TMPRSS3; MIR3197; TFF2; SNORA91; UMODL1; GET1-SH3BGR; PSMG1; PDE9A; RPS26P4; BRWD1-AS2; LINC00479; PDE9A-AS1; LOC105372813; LOC107985502; FAM3B; BRWD1; PCBP2P1; UBASH3A; MIR6814; ABCG1; LOC105369294; RSPH1; PRDM15; LINC02943; HMGN1; LOC107985478; LINC00111; LOC105372815; LOC105372812; LOC107987299; ZBTB21; DSCAM-AS1; TIMM9P2; ZNF295-AS1; RIPK4; RNU6-1149P; C2CD2; YRDCP3; PLAC4; LINC02940; JCADP1; SH3BGR; B3GALT5-AS1; BRWD1-AS1; RNF6P1; LCA5L; TFF1; LOC102724800; LINC00323; B3GALT5; SLC37A1; RNA5SP492; LOC105372809; BACE2; GET1; LINC01671; DSCAM; UMODL1-AS1; TMPRSS2; IGSF5; MIR6508; TFF3; See more...

Location information:

Clinical significance:

ID:: 48470470

variant

20.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: LOC101928255; RRP1B; LINC00319; TFF2; LOC101928212; TMPRSS3; MIR3197; H2BC12L; MX1; CBS; LOC105372815; LINC00322; LOC105372821; RSPH1; LOC107987299; ZBTB21; LOC101928369; SIK1; LOC107985504; LOC107985478; LOC105372812; RPL31P1; LINC00323; LINC00111; LOC105372809; PLAC4; PRDM15; MIR6814; LINC03039; ABCG1; MRPL51P2; LOC102723380; C2CD2; TFF1; LINC00313; LOC102724800; CRYAA; LINC01668; ZNF295-AS1; RIPK4; LOC105372814; YRDCP3; PKNOX1; RSPH1-DT; RNU6-1149P; LOC105372817; PCSEAT; UMODL1-AS1; BACE2; LINC01671; TFF3; MX2; LINC00112; FRGCA; LINC01679; ERVH48-1; FAM3B; DSCAM; MIR6070; LOC107987300; TMPRSS2; SLC37A1; PDE9A; LOC107985502; RNA5SP492; SNORA91; MIR5692B; UBASH3A; HSF2BP; UMODL1; NDUFV3; WDR4; LINC00479; LOC105372813; U2AF1; PDE9A-AS1; See more...

Location information:

Clinical significance:

ID:: 54356288

variant

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bace2[All Fields] AND 1[has_clinical] (58)
dbVar
Thalassiosira pseudonana CCMP1335 predicted protein mRNA
Thalassiosira pseudonana CCMP1335 predicted protein mRNA
gi|224009330|ref|XM_002293588.1|

Nucleotide
predicted protein [Thalassiosira pseudonana CCMP1335]
predicted protein [Thalassiosira pseudonana CCMP1335]
gi|224009331|ref|XP_002293624.1|

Protein

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