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Items: 1 to 20 of 183

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978819inversion1nstd209human GRCh38 chr15: 81,455,809-83,007,946 , GRCh37.p13 chr15: 81,748,150-83,676,698 RPS17, AP3B2, 39 more genes
    nsv5928313copy number variation1nstd209human GRCh38 chr15: 82,824,481-82,824,625 , GRCh37.p13 chr15: 83,493,233-83,493,377 WHAMM
    nsv5519465copy number variation1nstd206human GRCh38 chr15: 82,815,109-82,815,164 , GRCh37.p13 chr15: 83,483,861-83,483,916 WHAMM
    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
    nsv5146224mobile element insertion1nstd203human GRCh38 chr15: 82,815,091-82,815,103 , GRCh37.p13 chr15: 83,483,843-83,483,855 WHAMM
    nsv5002047copy number variation1nstd200human GRCh38 chr15: 82,834,967-82,837,132 , GRCh37.p13 chr15: 83,503,719-83,505,884 HOMER2, WHAMM
    nsv5002046copy number variation1nstd200human GRCh38 chr15: 82,821,728-82,823,986 , GRCh37.p13 chr15: 83,490,480-83,492,738 WHAMM
    nsv5002045copy number variation1nstd200human GRCh38 chr15: 82,821,386-82,821,476 , GRCh37.p13 chr15: 83,490,138-83,490,228 WHAMM
    nsv4856087copy number variation1nstd200human GRCh37 chr15: 83,490,479-83,492,738 , GRCh38.p12 chr15: 82,821,727-82,823,986 WHAMM
    nsv4729284copy number variation1nstd102humanPathogenic GRCh37 chr15: 83,201,955-85,786,847 , GRCh38.p12 chr15: 82,641,775-85,243,616 GOLGA6L5P, DNM1P44, 77 more genes
    nsv4630241copy number variation1nstd183human GRCh37 chr15: 83,486,959-83,491,918 , GRCh38.p12 chr15: 82,818,207-82,823,166 WHAMM
    nsv4629308copy number variation1nstd183human GRCh37 chr15: 83,486,842-83,488,286 , GRCh38.p12 chr15: 82,818,090-82,819,534 WHAMM
    nsv4623530copy number variation1nstd183human GRCh37 chr15: 83,478,070-83,486,781 , GRCh38.p12 chr15: 82,809,318-82,818,029 WHAMM
    nsv4578262copy number variation1nstd102humanPathogenic GRCh37 chr15: 83,214,012-84,772,030 , GRCh38.p12 chr15: 82,641,775-84,103,278 LOC100421235, LOC105370933, 29 more genes
    nsv4456897copy number variation1nstd102humanUncertain significance GRCh37 chr15: 82,468,371-84,797,068 , GRCh38.p12 chr15: 82,176,030-84,128,316 HDGFL3, LOC105370926, 46 more genes
    nsv4456639copy number variation1nstd102humanPathogenic GRCh37 chr15: 80,728,654-84,107,646 , GRCh38.p12 chr15: 80,436,313-83,438,894 LOC100288241, LOC105370926, 64 more genes
    nsv4455892copy number variation1nstd102humanPathogenic GRCh37 chr15: 82,688,216-84,796,779 , GRCh38.p12 chr15: 82,396,005-84,128,027 UBE2Q2P2, GOLGA2P10, 40 more genes
    nsv4247957copy number variation1nstd166human GRCh37.p13 chr15: 83,483,861-83,483,916 , GRCh38.p12 chr15: 82,815,109-82,815,164 WHAMM
    nsv4242108copy number variation1nstd166human GRCh37.p13 chr15: 83,483,876-83,484,083 , GRCh38.p12 chr15: 82,815,124-82,815,331 WHAMM
    nsv4241881copy number variation1nstd166human GRCh37.p13 chr15: 83,490,480-83,492,738 , GRCh38.p12 chr15: 82,821,728-82,823,986 WHAMM
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