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Items: 1 to 20 of 181

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5952252insertion1nstd209human GRCh38 chr7: 116,555,477-116,555,477 , GRCh37.p13 chr7: 116,195,531-116,195,531 CAV1
    nsv5949728insertion1nstd209human GRCh38 chr7: 116,534,384-116,534,384 , GRCh37.p13 chr7: 116,174,438-116,174,438 CAV1
    nsv5907702copy number variation1nstd209human GRCh38 chr7: 116,536,707-116,537,025 , GRCh37.p13 chr7: 116,176,761-116,177,079 CAV1
    nsv5573488copy number variation1nstd207human GRCh38 chr7: 116,555,477-116,555,539 , GRCh37.p13 chr7: 116,195,531-116,195,593 CAV1
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5554120sequence alteration1nstd206human GRCh38 chr7: 116,533,375-116,534,288 , GRCh37.p13 chr7: 116,173,429-116,174,342 CAV1
    nsv5488695copy number variation1nstd206human GRCh38 chr7: 116,557,619-116,558,016 , GRCh37.p13 chr7: 116,197,673-116,198,070 CAV1
    nsv5488595copy number variation1nstd206human GRCh38 chr7: 116,532,581-116,534,402 , GRCh37.p13 chr7: 116,172,635-116,174,456 CAV1
    nsv5483428copy number variation1nstd206human GRCh38 chr7: 116,545,989-116,546,044 , GRCh37.p13 chr7: 116,186,043-116,186,098 CAV1
    nsv5381457copy number variation1nstd102humanUncertain significance GRCh37 chr7: 116,166,573-116,166,573 , GRCh38.p12 chr7: 116,526,519-116,526,519 CAV1
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5118364mobile element insertion1nstd203human GRCh38 chr7: 116,534,395-116,534,417 , GRCh37.p13 chr7: 116,174,449-116,174,471 CAV1
    nsv5118026mobile element insertion1nstd203human GRCh38 chr7: 116,534,384-116,534,395 , GRCh37.p13 chr7: 116,174,438-116,174,449 CAV1
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4951137copy number variation1nstd200human GRCh38 chr7: 116,551,597-116,555,577 , GRCh37.p13 chr7: 116,191,651-116,195,631 CAV1
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4820214copy number variation1nstd200human GRCh37 chr7: 116,194,467-116,196,488 , GRCh38.p12 chr7: 116,554,413-116,556,434 CAV1
    nsv4675620copy number variation1nstd102humanPathogenic GRCh37 chr7: 109,251,060-159,119,707 , GRCh38.p12 chr7: 109,611,003-159,327,017 RPL26P23, ST13P17, 887 more genes
    nsv4675322copy number variation1nstd102humanPathogenic GRCh37 chr7: 106,617,406-123,217,914 , GRCh38.p12 chr7: 106,976,961-123,577,860 CBLL1-AS1, COMETT, 168 more genes
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