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Items: 1 to 20 of 213

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6913199copy number variation1nstd229human GRCh38 chr11: 78,115,131-78,115,575 , GRCh37.p13 chr11: 77,826,177-77,826,621 ALG8
    nsv6911136copy number variation1nstd229human GRCh38 chr11: 78,115,859-78,257,071 , GRCh37.p13 chr11: 77,826,905-77,968,117 RNU6-126P, USP35, 4 more genes
    nsv6907886copy number variation1nstd229human GRCh38 chr11: 78,122,557-78,131,998 , GRCh37.p13 chr11: 77,833,603-77,843,044 RNU6-126P, ALG8
    nsv6907617copy number variation1nstd229human GRCh38 chr11: 78,105,216-78,114,903 , GRCh37.p13 chr11: 77,816,262-77,825,949 ALG8
    nsv6903683copy number variation1nstd229human GRCh38 chr11: 78,132,145-78,134,532 , GRCh37.p13 chr11: 77,843,191-77,845,578 ALG8, RNU6-126P
    nsv6898191copy number variation1nstd229human GRCh38 chr11: 78,117,335-78,128,249 , GRCh37.p13 chr11: 77,828,381-77,839,295 ALG8
    nsv6637911copy number variation1nstd102humanUncertain significance GRCh37 chr11: 77,211,136-78,014,355 , GRCh38.p12 chr11: 77,500,091-78,303,309 RPS20P27, RNU7-59P, 22 more genes
    nsv6591070inversion1nstd223human GRCh38 chr11: 78,128,823-78,129,118 , GRCh37.p13 chr11: 77,839,869-77,840,164 ALG8
    nsv6585503inversion1nstd223human GRCh38 chr11: 78,122,451-78,123,036 , GRCh37.p13 chr11: 77,833,497-77,834,082 ALG8
    nsv6580346inversion1nstd223human GRCh38 chr11: 78,105,961-78,108,024 , GRCh37.p13 chr11: 77,817,007-77,819,070 ALG8
    nsv6580032inversion1nstd223human GRCh38 chr11: 78,115,459-78,116,438 , GRCh37.p13 chr11: 77,826,505-77,827,484 ALG8
    nsv6575631inversion1nstd223human GRCh38 chr11: 78,118,295-78,119,720 , GRCh37.p13 chr11: 77,829,341-77,830,766 ALG8
    nsv6474567copy number variation1nstd223human GRCh38 chr11: 78,117,328-78,128,241 , GRCh37.p13 chr11: 77,828,374-77,839,287 ALG8
    nsv6471306copy number variation1nstd223human GRCh38 chr11: 78,115,223-78,115,574 , GRCh37.p13 chr11: 77,826,269-77,826,620 ALG8
    nsv6465536copy number variation1nstd223human GRCh38 chr11: 78,138,866-78,139,775 , GRCh37.p13 chr11: 77,849,912-77,850,821 KCTD21-AS1, ALG8
    nsv6464943copy number variation1nstd223human GRCh38 chr11: 78,101,414-78,103,063 , GRCh37.p13 chr11: 77,812,460-77,814,109 ALG8
    nsv6463063copy number variation1nstd223human GRCh38 chr11: 78,132,997-78,134,298 , GRCh37.p13 chr11: 77,844,043-77,845,344 RNU6-126P, ALG8
    nsv6462020copy number variation1nstd223human GRCh38 chr11: 78,105,211-78,114,897 , GRCh37.p13 chr11: 77,816,257-77,825,943 ALG8
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6201623copy number variation1nstd214human GRCh38 chr11: 78,117,491-78,117,557 , GRCh37.p13 chr11: 77,828,537-77,828,603 ALG8
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