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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098217copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chrX: 117,629,935-119,761,021 , GRCh38.p12 chrX: 118,495,972-120,627,166 HNRNPA1P28, RNU7-86P, 59 more genes
    nsv7083163copy number variation1nstd229human GRCh38 chrX: 119,375,079-119,401,152 , GRCh37.p13 chrX: 118,509,042-118,535,115 MRPS17P9, SLC25A43
    nsv7083161copy number variation1nstd229human GRCh38 chrX: 119,372,590-119,428,791 , GRCh37.p13 chrX: 118,506,553-118,562,754 RNU1-67P, MRPS17P9, 1 more genes
    nsv7083160copy number variation1nstd229human GRCh38 chrX: 119,367,150-119,433,099 , GRCh37.p13 chrX: 118,501,113-118,567,062 RN7SL118P, MRPS17P9, 2 more genes
    nsv7083159copy number variation1nstd229human GRCh38 chrX: 119,362,707-119,388,924 , GRCh37.p13 chrX: 118,496,670-118,522,887 MRPS17P9
    nsv7083158copy number variation1nstd229human GRCh38 chrX: 119,361,411-119,565,034 , GRCh37.p13 chrX: 118,495,374-118,698,997 STEEP1, SLC25A43, 6 more genes
    nsv7083157copy number variation1nstd229human GRCh38 chrX: 119,361,012-119,422,294 , GRCh37.p13 chrX: 118,494,975-118,556,257 MRPS17P9, RNU1-67P, 1 more genes
    nsv7083152copy number variation1nstd229human GRCh38 chrX: 119,344,550-119,416,446 , GRCh37.p13 chrX: 118,478,513-118,550,409 SLC25A43, MRPS17P9
    nsv7083145copy number variation1nstd229human GRCh38 chrX: 119,322,120-119,423,681 , GRCh37.p13 chrX: 118,456,083-118,557,644 LINC03098, MRPS17P9, 2 more genes
    nsv7083140copy number variation1nstd229human GRCh38 chrX: 119,302,372-119,397,838 , GRCh37.p13 chrX: 118,436,335-118,531,801 LINC03098, SLC25A43, 1 more genes
    nsv7083133copy number variation1nstd229human GRCh38 chrX: 119,283,254-119,415,717 , GRCh37.p13 chrX: 118,417,217-118,549,680 LINC03098, MRPS17P9, 1 more genes
    nsv7083100copy number variation1nstd229human GRCh38 chrX: 119,244,582-119,503,676 , GRCh37.p13 chrX: 118,378,545-118,637,639 SLC25A5-AS1, SLC25A5, 8 more genes
    nsv7057233inversion1nstd229human GRCh38 chrX: 117,599,215-122,918,174 , GRCh37.p13 chrX: 116,733,178-122,052,027 NUDT19P1, RHOXF1P2, 89 more genes
    nsv7055271inversion1nstd229human GRCh38 chrX: 114,091,775-119,749,531 , GRCh37.p13 chrX: 115,732,291-118,883,494 ZCCHC12, CT47C1, 83 more genes
    nsv7053106inversion1nstd229human GRCh38 chrX: 118,857,141-120,493,178 , GRCh37.p13 chrX: 117,991,104-119,627,033 LINC03098, RNF113A, 49 more genes
    nsv7049773inversion1nstd229human GRCh38 chrX: 118,660,648-122,841,710 , GRCh37.p13 chrX: 117,794,611-121,975,563 NUDT19P6, MRPS17P9, 83 more genes
    nsv7040757inversion1nstd229human GRCh38 chrX: 119,358,756-119,946,578 , GRCh37.p13 chrX: 118,492,719-119,080,541 NDUFA1, UBE2A, 20 more genes
    nsv7038305inversion1nstd229human GRCh38 chrX: 118,464,002-122,855,541 , GRCh37.p13 chrX: 117,597,965-121,989,394 UBE2V1P16, RNY3P16, 84 more genes
    nsv6637078copy number variation1nstd102humanUncertain significance GRCh37 chrX: 117,651,370-118,792,490 , GRCh38.p12 chrX: 118,517,407-119,658,527 LONRF3, CT47C1, 28 more genes
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