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Items: 1 to 20 of 241

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5887392copy number variation1nstd209human GRCh38 chr2: 19,960,028-19,960,148 , GRCh37.p13 chr2: 20,159,789-20,159,909 WDR35
    nsv5870034copy number variation1nstd209human GRCh38 chr2: 19,980,237-19,980,493 , GRCh37.p13 chr2: 20,179,998-20,180,254 WDR35
    nsv5692563mobile element insertion1nstd211human GRCh38 chr2: 19,912,972-19,912,972 , GRCh37.p13 chr2: 20,112,733-20,112,733 WDR35
    nsv5690078mobile element insertion2nstd211human GRCh38 chr2: 19,977,678-19,977,678 , GRCh37.p13 chr2: 20,177,439-20,177,439 WDR35
    nsv5676465mobile element insertion1nstd211human GRCh38 chr2: 19,946,172-19,946,172 , GRCh37.p13 chr2: 20,145,933-20,145,933 WDR35
    nsv5624349insertion1nstd207human GRCh38 chr2: 19,985,275-19,985,275 , GRCh37.p13 chr2: 20,185,036-20,185,036 RNFT1P1, WDR35
    nsv5619283insertion1nstd207human GRCh38 chr2: 19,977,665-19,977,665 , GRCh37.p13 chr2: 20,177,426-20,177,426 WDR35
    nsv5406668mobile element insertion1nstd206human GRCh38 chr2: 19,977,678-19,977,684 , GRCh37.p13 chr2: 20,177,439-20,177,445 WDR35
    nsv5405031mobile element insertion1nstd206human GRCh38 chr2: 19,912,972-19,913,023 , GRCh37.p13 chr2: 20,112,733-20,112,784 WDR35
    nsv5400993mobile element insertion1nstd206human GRCh38 chr2: 19,946,172-19,946,223 , GRCh37.p13 chr2: 20,145,933-20,145,984 WDR35
    nsv5167622mobile element insertion1nstd203human GRCh38 chr2: 19,958,349-19,958,369 , GRCh37.p13 chr2: 20,158,110-20,158,130 WDR35
    nsv5075841mobile element insertion1nstd203human GRCh38 chr2: 19,946,153-19,946,172 , GRCh37.p13 chr2: 20,145,914-20,145,933 WDR35
    nsv5073725mobile element insertion1nstd203human GRCh38 chr2: 19,960,451-19,960,467 , GRCh37.p13 chr2: 20,160,212-20,160,228 WDR35
    nsv5063389mobile element insertion1nstd203human GRCh38 chr2: 19,977,665-19,977,678 , GRCh37.p13 chr2: 20,177,426-20,177,439 WDR35
    nsv4900509copy number variation1nstd200human GRCh38 chr2: 19,977,633-19,980,477 , GRCh37.p13 chr2: 20,177,394-20,180,238 WDR35
    nsv4788305copy number variation1nstd200human GRCh37 chr2: 20,179,998-20,180,257 , GRCh38.p12 chr2: 19,980,237-19,980,496 WDR35
    nsv4775667copy number variation1nstd200human GRCh37 chr2: 20,177,394-20,180,238 , GRCh38.p12 chr2: 19,977,633-19,980,477 WDR35
    nsv4728290copy number variation1nstd102humanUncertain significance GRCh37 chr2: 20,026,422-20,115,214 , GRCh38.p12 chr2: 19,826,661-19,915,453 TTC32, LINC00954, 2 more genes
    nsv4583170copy number variation1nstd183human GRCh37 chr2: 20,112,606-20,113,624 , GRCh38.p12 chr2: 19,912,845-19,913,863 WDR35
    nsv4564685mobile element insertion1nstd166human GRCh37.p13 chr2: 20,158,110-20,158,110 , GRCh38.p12 chr2: 19,958,349-19,958,349 WDR35
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