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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112765copy number variation1nstd102humanPathogenic GRCh37 chr10: 118,247,181-135,435,319 , GRCh38.p12 chr10: 116,487,669-133,621,815 STK32C, LOC105378542, 266 more genes
    nsv5980446copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,785,023-135,457,222 , GRCh38.p12 chr10: 121,025,510-133,643,718 LINC02641, CFAP46, 194 more genes
    nsv5967944insertion1nstd209human GRCh38 chr10: 126,576,659-126,576,659 , GRCh37.p13 chr10: 128,265,228-128,265,228 C10orf90
    nsv5926097copy number variation1nstd209human GRCh38 chr10: 126,588,143-126,598,130 , GRCh37.p13 chr10: 128,276,712-128,286,699 C10orf90
    nsv5916883copy number variation1nstd209human GRCh38 chr10: 126,565,190-126,565,248 , GRCh37.p13 chr10: 128,253,759-128,253,817 C10orf90
    nsv5864431copy number variation1nstd209human GRCh38 chr10: 126,442,780-126,445,086 , GRCh37.p13 chr10: 128,131,349-128,133,655 LOC728158, C10orf90
    nsv5849030copy number variation1nstd209human GRCh38 chr10: 126,588,113-126,598,163 , GRCh37.p13 chr10: 128,276,682-128,286,732 C10orf90
    nsv5727700mobile element insertion2nstd211human GRCh38 chr10: 126,477,118-126,477,118 , GRCh37.p13 chr10: 128,165,687-128,165,687 C10orf90
    nsv5724874mobile element insertion1nstd211human GRCh38 chr10: 126,425,145-126,425,145 , GRCh37.p13 chr10: 128,113,714-128,113,714 C10orf90, LOC728158, 1 more genes
    nsv5720137mobile element insertion1nstd211human GRCh38 chr10: 126,473,659-126,473,659 , GRCh37.p13 chr10: 128,162,228-128,162,228 C10orf90
    nsv5712479mobile element insertion2nstd211human GRCh38 chr10: 126,519,532-126,519,532 , GRCh37.p13 chr10: 128,208,101-128,208,101 C10orf90
    nsv5711883mobile element insertion1nstd211human GRCh38 chr10: 126,530,790-126,530,790 , GRCh37.p13 chr10: 128,219,359-128,219,359 C10orf90
    nsv5702294mobile element insertion2nstd211human GRCh38 chr10: 126,648,819-126,648,819 , GRCh37.p13 chr10: 128,337,388-128,337,388 C10orf90
    nsv5697835mobile element insertion2nstd211human GRCh38 chr10: 126,547,513-126,547,513 , GRCh37.p13 chr10: 128,236,082-128,236,082 C10orf90
    nsv5694607mobile element insertion1nstd211human GRCh38 chr10: 126,655,851-126,655,851 , GRCh37.p13 chr10: 128,344,420-128,344,420 C10orf90
    nsv5672526copy number variation1nstd102humanPathogenic GRCh37 chr10: 127,548,166-135,440,251 , GRCh38.p12 chr10: 125,859,597-133,626,747 LINC00601, RPL5P28, 110 more genes
    nsv5643934insertion1nstd207human GRCh38 chr10: 126,564,835-126,564,835 , GRCh37.p13 chr10: 128,253,404-128,253,404 C10orf90
    nsv5642147insertion1nstd207human GRCh38 chr10: 126,565,028-126,565,028 , GRCh37.p13 chr10: 128,253,597-128,253,597 C10orf90
    nsv5636793insertion1nstd207human GRCh38 chr10: 126,565,375-126,565,375 , GRCh37.p13 chr10: 128,253,944-128,253,944 C10orf90
    nsv5633830insertion1nstd207human GRCh38 chr10: 126,564,832-126,564,832 , GRCh37.p13 chr10: 128,253,401-128,253,401 C10orf90
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