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Items: 1 to 20 of 163

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977506insertion1nstd209human GRCh38 chr15: 76,953,570-76,953,570 , GRCh37.p13 chr15: 77,245,911-77,245,911 RCN2
    nsv5933606copy number variation1nstd209human GRCh38 chr15: 71,577,714-80,433,232 , GRCh37.p13 chr15: 71,870,053-80,725,573 , STRA6, 229 more genes
    nsv5516122copy number variation1nstd206human GRCh38 chr15: 76,953,557-76,953,770 , GRCh37.p13 chr15: 77,245,898-77,246,111 RCN2
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5312057copy number variation1nstd204human GRCh38.p13 chr15: 76,939,475-76,940,012 , GRCh37.p13 chr15: 77,231,816-77,232,353 RCN2
    nsv5153390mobile element insertion1nstd203human GRCh38 chr15: 76,953,754-76,953,761 , GRCh37.p13 chr15: 77,246,095-77,246,102 RCN2
    nsv5144446mobile element insertion1nstd203human GRCh38 chr15: 76,935,466-76,935,475 , GRCh37.p13 chr15: 77,227,807-77,227,816 RCN2
    nsv5141577mobile element insertion1nstd203human GRCh38 chr15: 76,953,593-76,953,625 , GRCh37.p13 chr15: 77,245,934-77,245,966 RCN2
    nsv5037756inversion1nstd200human GRCh38 chr15: 75,735,812-77,868,882 , GRCh37.p13 chr15: 76,028,153-78,161,224 TRK-CTT16-1, SCAPER, 34 more genes
    nsv5001830copy number variation1nstd200human GRCh38 chr15: 76,952,909-76,953,859 , GRCh37.p13 chr15: 77,245,250-77,246,200 RCN2
    nsv4992298copy number variation1nstd200human GRCh38 chr15: 73,152,590-82,101,178 , GRCh37.p13 chr15: 73,444,931-82,393,519 , SNUPN, 215 more genes
    nsv4850167copy number variation1nstd200human GRCh37 chr15: 77,245,239-77,246,186 , GRCh38.p12 chr15: 76,952,898-76,953,845 RCN2
    nsv4626375copy number variation1nstd183human GRCh37 chr15: 77,223,995-77,224,061 , GRCh38.p12 chr15: 76,931,654-76,931,720 RCN2
    nsv4624422copy number variation1nstd183human GRCh37 chr15: 77,233,892-77,236,077 , GRCh38.p12 chr15: 76,941,551-76,943,736 RCN2
    nsv4567783mobile element insertion1nstd166human GRCh37.p13 chr15: 77,241,862-77,241,862 , GRCh38.p12 chr15: 76,949,521-76,949,521 RCN2
    nsv4515312mobile element insertion1nstd166human GRCh37.p13 chr15: 77,242,255-77,242,255 , GRCh38.p12 chr15: 76,949,914-76,949,914 RCN2
    nsv4241390copy number variation1nstd166human GRCh37.p13 chr15: 77,245,898-77,246,111 , GRCh38.p12 chr15: 76,953,557-76,953,770 RCN2
    nsv3922157copy number variation1nstd102humanUncertain significance NCBI36 chr15: 29,852,369-100,338,915 , GRCh37.p13 chr15: 32,065,077-102,521,392 , GRCh38.p12 chr15: 31,772,874-101,981,189 GCHFR, SPPL2A, 1382 more genes
    nsv3919468copy number variation1nstd102humanPathogenic NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189 RNU6-18P, GOLGA8K, 1442 more genes
    nsv3918770copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,280,728-100,338,915 , GRCh37.p13 chr15: 22,729,364-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNRPCP18, SNORD116-30, 1622 more genes
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