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Items: 1 to 20 of 261

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137129copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,531,028-134,257,553 , GRCh38.p12 chr11: 120,660,319-134,387,659 VSIG10L2, OR8B6P, 268 more genes
    nsv7077728inversion1nstd229human GRCh38 chr11: 124,239,803-134,089,458 , GRCh37.p13 chr11: 124,110,545-133,959,353 LOC283172, PPP1R10P1, 175 more genes
    nsv7064476inversion1nstd229human GRCh38 chr11: 123,462,060-125,907,500 , GRCh37.p13 chr11: 123,332,768-125,777,395 STT3A, OR8G1, 101 more genes
    nsv6916100copy number variation1nstd229human GRCh38 chr11: 124,808,783-124,811,494 , GRCh37.p13 chr11: 124,678,679-124,681,390 MSANTD2-AS1, LOC107984357
    nsv6916077copy number variation1nstd229human GRCh38 chr11: 124,575,701-124,974,400 , GRCh37.p13 chr11: 124,445,597-124,844,296 SIAE, HEPACAM, 19 more genes
    nsv6911308copy number variation1nstd229human GRCh38 chr11: 124,828,435-124,836,769 , GRCh37.p13 chr11: 124,698,331-124,706,665 MSANTD2-AS1
    nsv6907226copy number variation1nstd229human GRCh38 chr11: 124,826,799-124,828,352 , GRCh37.p13 chr11: 124,696,695-124,698,248 MSANTD2-AS1
    nsv6907223copy number variation1nstd229human GRCh38 chr11: 124,833,586-124,837,186 , GRCh37.p13 chr11: 124,703,482-124,707,082 MSANTD2-AS1
    nsv6906284copy number variation1nstd229human GRCh38 chr11: 124,828,472-124,836,755 , GRCh37.p13 chr11: 124,698,368-124,706,651 MSANTD2-AS1
    nsv6903295copy number variation1nstd229human GRCh38 chr11: 124,828,817-124,829,178 , GRCh37.p13 chr11: 124,698,713-124,699,074 MSANTD2-AS1
    nsv6901151copy number variation1nstd229human GRCh38 chr11: 124,811,892-124,812,870 , GRCh37.p13 chr11: 124,681,788-124,682,766 MSANTD2-AS1
    nsv6899803copy number variation1nstd229human GRCh38 chr11: 124,826,549-124,826,575 , GRCh37.p13 chr11: 124,696,445-124,696,471 MSANTD2-AS1
    nsv6899698copy number variation1nstd229human GRCh38 chr11: 124,815,001-124,816,800 , GRCh37.p13 chr11: 124,684,897-124,686,696 MSANTD2-AS1
    nsv6637558copy number variation1nstd102humanPathogenic GRCh37 chr11: 122,975,824-134,938,470 , GRCh38.p12 chr11: 123,105,116-135,068,576 OR8B8, LOC107984373, 234 more genes
    nsv6578273inversion1nstd223human GRCh38 chr11: 124,827,531-124,828,328 , GRCh37.p13 chr11: 124,697,427-124,698,224 MSANTD2-AS1
    nsv6471461copy number variation1nstd223human GRCh38 chr11: 124,808,783-124,811,489 , GRCh37.p13 chr11: 124,678,679-124,681,385 MSANTD2-AS1, LOC107984357
    nsv6458856copy number variation1nstd223human GRCh38 chr11: 124,811,892-124,812,870 , GRCh37.p13 chr11: 124,681,788-124,682,766 MSANTD2-AS1
    nsv6457906copy number variation1nstd223human GRCh38 chr11: 124,828,419-124,836,760 , GRCh37.p13 chr11: 124,698,315-124,706,656 MSANTD2-AS1
    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
    nsv6309036copy number variation3nstd102humanUncertain significance GRCh37 chr11: 123,504,851-126,163,012 , GRCh38.p12 chr11: 123,634,143-126,293,117 CDON, PKNOX2-DT, 113 more genes
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