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Items: 1 to 20 of 951

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148201copy number variation1nstd102humanPathogenic GRCh38 chr3: 93,979,547-124,774,010 , GRCh37.p13 chr3: 93,698,391-124,492,857 NECTIN3, H2BP3, 418 more genes
    nsv7057000inversion1nstd229human GRCh38 chr3: 121,127,606-121,127,671 , GRCh37.p13 chr3: 120,846,453-120,846,518 STXBP5L
    nsv7056993inversion1nstd229human GRCh38 chr3: 121,203,602-121,203,706 , GRCh37.p13 chr3: 120,922,449-120,922,553 STXBP5L
    nsv7054524inversion1nstd229human GRCh38 chr3: 121,238,043-121,240,728 , GRCh37.p13 chr3: 120,956,890-120,959,575 STXBP5L
    nsv7053411inversion1nstd229human GRCh38 chr3: 121,343,867-121,347,588 , GRCh37.p13 chr3: 121,062,714-121,066,435 STXBP5L
    nsv7052355inversion1nstd229human GRCh38 chr3: 120,955,810-120,959,657 , GRCh37.p13 chr3: 120,674,657-120,678,504 STXBP5L
    nsv7051171inversion1nstd229human GRCh38 chr3: 121,271,249-121,271,338 , GRCh37.p13 chr3: 120,990,096-120,990,185 STXBP5L
    nsv7050714inversion1nstd229human GRCh38 chr3: 119,886,071-121,104,541 , GRCh37.p13 chr3: 119,604,918-120,823,388 PARLP1, LOC105374069, 26 more genes
    nsv7047926inversion1nstd229human GRCh38 chr3: 121,053,406-121,092,210 , GRCh37.p13 chr3: 120,772,253-120,811,057 STXBP5L
    nsv7044866inversion1nstd229human GRCh38 chr3: 121,237,837-121,244,853 , GRCh37.p13 chr3: 120,956,684-120,963,700 STXBP5L
    nsv7041905inversion1nstd229human GRCh38 chr3: 121,021,784-121,035,775 , GRCh37.p13 chr3: 120,740,631-120,754,622 STXBP5L
    nsv7041333inversion1nstd229human GRCh38 chr3: 119,602,733-121,708,334 , GRCh37.p13 chr3: 119,321,580-121,427,181 RABL3, PTOV1P1, 44 more genes
    nsv7041004inversion1nstd229human GRCh38 chr3: 121,168,688-121,350,654 , GRCh37.p13 chr3: 120,887,535-121,069,501 STXBP5L
    nsv7039920inversion1nstd229human GRCh38 chr3: 119,602,735-121,711,940 , GRCh37.p13 chr3: 119,321,582-121,430,787 LINC02049, GSK3B, 44 more genes
    nsv6717932copy number variation1nstd229human GRCh38 chr3: 120,917,546-120,922,033 , GRCh37.p13 chr3: 120,636,393-120,640,880 STXBP5L
    nsv6717767copy number variation1nstd229human GRCh38 chr3: 121,179,433-121,181,872 , GRCh37.p13 chr3: 120,898,280-120,900,719 STXBP5L
    nsv6717637copy number variation1nstd229human GRCh38 chr3: 121,170,757-121,173,903 , GRCh37.p13 chr3: 120,889,604-120,892,750 STXBP5L
    nsv6717605copy number variation1nstd229human GRCh38 chr3: 121,301,909-121,306,725 , GRCh37.p13 chr3: 121,020,756-121,025,572 STXBP5L
    nsv6717217copy number variation1nstd229human GRCh38 chr3: 121,226,507-121,231,164 , GRCh37.p13 chr3: 120,945,354-120,950,011 STXBP5L
    nsv6716986copy number variation1nstd229human GRCh38 chr3: 121,359,461-121,365,725 , GRCh37.p13 chr3: 121,078,308-121,084,572 STXBP5L
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