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Items: 1 to 20 of 413

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976704inversion1nstd209human GRCh38 chr20: 36,955,252-45,585,469 , GRCh37.p13 chr20: 35,583,655-44,214,108 , ADA, 180 more genes
    nsv5966329copy number variation1nstd209human GRCh38 chr20: 44,157,818-44,157,888 , GRCh37.p13 chr20: 42,786,458-42,786,528 JPH2
    nsv5965884copy number variation1nstd209human GRCh38 chr20: 44,161,632-44,162,205 , GRCh37.p13 chr20: 42,790,272-42,790,845 JPH2
    nsv5962279copy number variation1nstd209human GRCh38 chr20: 44,133,900-44,134,043 , GRCh37.p13 chr20: 42,762,540-42,762,683 JPH2
    nsv5961534copy number variation1nstd209human GRCh38 chr20: 44,133,951-44,134,223 , GRCh37.p13 chr20: 42,762,591-42,762,863 JPH2
    nsv5873115copy number variation1nstd209human GRCh38 chr20: 44,169,181-44,193,840 , GRCh37.p13 chr20: 42,797,821-42,822,480 JPH2
    nsv5695576mobile element insertion2nstd211human GRCh38 chr20: 44,162,745-44,162,745 , GRCh37.p13 chr20: 42,791,385-42,791,385 JPH2
    nsv5669995insertion1nstd207human GRCh38 chr20: 44,134,679-44,134,679 , GRCh37.p13 chr20: 42,763,319-42,763,319 JPH2
    nsv5669731insertion1nstd207human GRCh38 chr20: 44,134,139-44,134,139 , GRCh37.p13 chr20: 42,762,779-42,762,779 JPH2
    nsv5669514insertion1nstd207human GRCh38 chr20: 44,134,614-44,134,614 , GRCh37.p13 chr20: 42,763,254-42,763,254 JPH2
    nsv5669091insertion1nstd207human GRCh38 chr20: 44,134,325-44,134,325 , GRCh37.p13 chr20: 42,762,965-42,762,965 JPH2
    nsv5667818insertion1nstd207human GRCh38 chr20: 44,133,946-44,133,946 , GRCh37.p13 chr20: 42,762,586-42,762,586 JPH2
    nsv5667569insertion1nstd207human GRCh38 chr20: 44,134,467-44,134,467 , GRCh37.p13 chr20: 42,763,107-42,763,107 JPH2
    nsv5664886insertion1nstd207human GRCh38 chr20: 44,135,089-44,135,089 , GRCh37.p13 chr20: 42,763,729-42,763,729 JPH2
    nsv5664885insertion2nstd207human GRCh38 chr20: 44,132,792-44,132,792 , GRCh37.p13 chr20: 42,761,432-42,761,432 JPH2
    nsv5664660insertion1nstd207human GRCh38 chr20: 44,126,168-44,126,168 , GRCh37.p13 chr20: 42,754,808-42,754,808 JPH2
    nsv5603896copy number variation1nstd207human GRCh38 chr20: 44,134,620-44,134,725 , GRCh37.p13 chr20: 42,763,260-42,763,365 JPH2
    nsv5600963copy number variation1nstd207human GRCh38 chr20: 44,133,948-44,134,063 , GRCh37.p13 chr20: 42,762,588-42,762,703 JPH2
    nsv5595509copy number variation1nstd207human GRCh38 chr20: 44,133,833-44,133,883 , GRCh37.p13 chr20: 42,762,473-42,762,523 JPH2
    nsv5594194copy number variation1nstd207human GRCh38 chr20: 44,134,010-44,134,561 , GRCh37.p13 chr20: 42,762,650-42,763,201 JPH2
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