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Items: 1 to 20 of 105

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5314034copy number variation1nstd204human GRCh37.p13 chr15: 62,582,863-62,613,588 , GRCh38.p13 chr15: 62,290,664-62,321,389 , MIR8067
    nsv5263022copy number variation1nstd204human GRCh38.p13 chr15: 62,290,318-62,302,960 , GRCh37.p13 chr15: 62,582,517-62,595,159 , MIR8067
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 more genes
    nsv5005484copy number variation1nstd200human GRCh38 chr15: 62,273,337-62,386,849 , GRCh37.p13 chr15: 62,565,536-62,679,048 , LOC102724938, 3 more genes
    nsv5005479copy number variation1nstd200human GRCh38 chr15: 61,919,879-62,306,634 , GRCh37.p13 chr15: 62,212,078-62,598,833 , VPS13C-DT, 9 more genes
    nsv4872280inversion1nstd200human GRCh37 chr15: 40,414,149-64,343,008 , GRCh38.p12 chr15: 40,121,948-64,050,809 , DNAAF4-CCPG1, 475 more genes
    nsv4863840copy number variation1nstd200human GRCh37 chr15: 62,565,536-62,679,048 , GRCh38.p12 chr15: 62,273,337-62,386,849 , MIR6085, 3 more genes
    nsv4849771copy number variation1nstd200human GRCh37 chr15: 62,582,871-62,613,580 , GRCh38.p12 chr15: 62,290,672-62,321,381 , MIR8067
    nsv4675468copy number variation1nstd102humanUncertain significance GRCh37 chr15: 62,398,532-62,626,845 , GRCh38.p12 chr15: 62,106,333-62,334,646 LOC107984784, GOLGA2P11, 3 more genes
    nsv4631747copy number variation1nstd183human GRCh37 chr15: 62,587,474-62,610,231 , GRCh38.p12 chr15: 62,295,275-62,318,032 , MIR8067
    nsv4243945copy number variation1nstd166human GRCh37.p13 chr15: 62,212,078-62,598,784 , GRCh38.p12 chr15: 61,919,879-62,306,585 , GOLGA2P11, 9 more genes
    nsv4240070copy number variation1nstd166human GRCh37.p13 chr15: 62,584,998-62,907,277 , GRCh38.p12 chr15: 62,292,799-62,615,078 , HMGN1P26, 3 more genes
    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
    nsv3921425copy number variation1nstd102humanPathogenic NCBI36 chr15: 55,647,440-61,098,667 , GRCh37 chr15: 57,860,148-63,311,614 , GRCh38 chr15: 57,567,950-63,019,415 MESTP2, HMGB1P51, 86 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
    nsv3918644copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,313,935-100,338,915 , GRCh37.p13 chr15: 22,762,571-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNORD116-23, UBE2Q2P6, 1622 more genes
    nsv3917589copy number variation1nstd102humanPathogenic GRCh37 chr15: 60,120,659-102,461,201 , GRCh38 chr15: 59,828,460-101,920,998 , NCBI36 chr15: 57,907,951-100,278,724 GAPDHP61, SNORD18B, 840 more genes
    nsv3916249copy number variation1nstd102humanPathogenic NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189 H3P40, EEF1B2P1, 1616 more genes
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