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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5918885copy number variation1nstd209human GRCh38 chr10: 74,132,308-74,133,922 , GRCh37.p13 chr10: 75,892,066-75,893,680 AP3M1
    nsv5911661copy number variation1nstd209human GRCh38 chr10: 74,139,587-74,143,155 , GRCh37.p13 chr10: 75,899,345-75,902,913 AP3M1
    nsv5909992copy number variation1nstd209human GRCh38 chr10: 72,964,663-80,533,256 , GRCh37.p13 chr10: 74,724,421-82,293,012 , PRXL2A, 155 more genes
    nsv5859041copy number variation1nstd209human GRCh38 chr10: 74,132,287-74,133,986 , GRCh37.p13 chr10: 75,892,045-75,893,744 AP3M1
    nsv5847752copy number variation1nstd209human GRCh38 chr10: 74,139,731-74,143,155 , GRCh37.p13 chr10: 75,899,489-75,902,913 AP3M1
    nsv5695112mobile element insertion2nstd211human GRCh38 chr10: 74,141,478-74,141,478 , GRCh37.p13 chr10: 75,901,236-75,901,236 AP3M1
    nsv5599094copy number variation1nstd207human GRCh38 chr10: 74,139,370-74,141,203 , GRCh37.p13 chr10: 75,899,128-75,900,961 AP3M1
    nsv5485217copy number variation1nstd206human GRCh38 chr10: 74,139,595-74,143,106 , GRCh37.p13 chr10: 75,899,353-75,902,864 AP3M1
    nsv5474422copy number variation1nstd206human GRCh38 chr10: 74,139,417-74,141,197 , GRCh37.p13 chr10: 75,899,175-75,900,955 AP3M1
    nsv5401258mobile element insertion1nstd206human GRCh38 chr10: 74,141,478-74,141,529 , GRCh37.p13 chr10: 75,901,236-75,901,287 AP3M1
    nsv5301974copy number variation1nstd204human GRCh38.p13 chr10: 73,709,242-74,768,785 , GRCh37.p13 chr10: 75,469,000-76,528,543 , RPSAP6, 24 more genes
    nsv5248085copy number variation1nstd204human GRCh38.p13 chr10: 74,116,618-74,196,286 , GRCh37.p13 chr10: 75,876,376-75,956,044 VCL, ADK, 1 more genes
    nsv5245630copy number variation1nstd204human GRCh38.p13 chr10: 74,134,587-74,136,949 , GRCh37.p13 chr10: 75,894,345-75,896,707 AP3M1
    nsv5133774mobile element insertion1nstd203human GRCh38 chr10: 74,127,634-74,127,677 , GRCh37.p13 chr10: 75,887,392-75,887,435 AP3M1
    nsv5125142mobile element insertion1nstd203human GRCh38 chr10: 74,126,970-74,127,001 , GRCh37.p13 chr10: 75,886,728-75,886,759 AP3M1
    nsv5124101mobile element insertion1nstd203human GRCh38 chr10: 74,126,984-74,127,000 , GRCh37.p13 chr10: 75,886,742-75,886,758 AP3M1
    nsv5120903mobile element insertion1nstd203human GRCh38 chr10: 74,141,461-74,141,478 , GRCh37.p13 chr10: 75,901,219-75,901,236 AP3M1
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4976546copy number variation1nstd200human GRCh38 chr10: 74,141,334-74,174,058 , GRCh37.p13 chr10: 75,901,092-75,933,816 ADK, AP3M1
    nsv4976545copy number variation1nstd200human GRCh38 chr10: 74,139,564-74,143,151 , GRCh37.p13 chr10: 75,899,322-75,902,909 AP3M1
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