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Items: 1 to 20 of 118

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7062479inversion1nstd229human GRCh38 chr11: 78,062,853-78,080,770 , GRCh37.p13 chr11: 77,773,899-77,791,816 THRSP, NDUFC2-KCTD14, 2 more genes
    nsv6905682copy number variation1nstd229human GRCh38 chr11: 77,702,101-78,075,000 , GRCh37.p13 chr11: 77,413,146-77,786,046 FTH1P16, AAMDC, 8 more genes
    nsv6902160copy number variation1nstd229human GRCh38 chr11: 78,062,563-78,065,420 , GRCh37.p13 chr11: 77,773,609-77,776,466 THRSP, NDUFC2-KCTD14
    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
    nsv6621021copy number variation1nstd224human GRCh37 chr11: 77,413,223-77,785,836 , GRCh38.p12 chr11: 77,702,178-78,074,790 NDUFC2, AAMDC, 8 more genes
    nsv6463092copy number variation1nstd223human GRCh38 chr11: 77,925,634-78,075,013 , GRCh37.p13 chr11: 77,636,680-77,786,059 KCTD14, NDUFC2-KCTD14, 3 more genes
    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
    nsv6112766copy number variation1nstd102humannot provided GRCh37 chr11: 77,617,820-77,784,237 , GRCh38.p12 chr11: 77,906,774-78,073,191 KCTD14, NDUFC2-KCTD14, 3 more genes
    nsv5907740copy number variation1nstd209human GRCh38 chr11: 78,068,581-78,068,920 , GRCh37.p13 chr11: 77,779,627-77,779,966 NDUFC2, THRSP, 1 more genes
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv4989069copy number variation1nstd200human GRCh38 chr11: 77,925,632-78,075,017 , GRCh37.p13 chr11: 77,636,678-77,786,063 INTS4, NDUFC2, 3 more genes
    nsv4989067copy number variation1nstd200human GRCh38 chr11: 77,839,766-78,289,807 , GRCh37.p13 chr11: 77,550,812-78,000,853 KCTD21-AS1, NDUFC2, 13 more genes
    nsv4844562copy number variation1nstd200human GRCh37 chr11: 77,779,629-77,779,967 , GRCh38.p12 chr11: 78,068,583-78,068,921 NDUFC2, THRSP, 1 more genes
    nsv4842769copy number variation1nstd200human GRCh37 chr11: 77,550,812-78,000,853 , GRCh38.p12 chr11: 77,839,766-78,289,807 KCTD14, THRSP, 13 more genes
    nsv4729234copy number variation1nstd102humanUncertain significance GRCh37 chr11: 77,575,261-77,902,589 , GRCh38.p12 chr11: 77,864,215-78,191,543 LOC105369401, KCTD21, 12 more genes
    nsv4455314copy number variation2nstd102humanUncertain significance GRCh37 chr11: 77,410,575-77,785,783 , GRCh38.p12 chr11: 77,699,530-78,074,737 FTH1P16, AAMDC, 8 more genes
    nsv4381100copy number variation1nstd173human GRCh37 chr11: 77,643,952-77,834,894 , GRCh38.p12 chr11: 77,932,906-78,123,848 KCTD14, NDUFC2-KCTD14, 5 more genes
    nsv4377670copy number variation1nstd173human GRCh37 chr11: 77,639,679-77,834,894 , GRCh38.p12 chr11: 77,928,633-78,123,848 NDUFC2, ALG8, 5 more genes
    nsv4199332copy number variation1nstd166human GRCh37.p13 chr11: 77,768,678-77,776,567 , GRCh38.p12 chr11: 78,057,632-78,065,521 NDUFC2-KCTD14, THRSP
    nsv4196428copy number variation1nstd166human GRCh37.p13 chr11: 77,636,680-77,786,061 , GRCh38.p12 chr11: 77,925,634-78,075,015 NDUFC2, THRSP, 3 more genes
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