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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6917685copy number variation1nstd229human GRCh38 chr11: 77,689,948-77,872,635 , GRCh37.p13 chr11: 77,400,993-77,583,681 INTS4, RSF1, 4 more genes
    nsv6913160copy number variation1nstd229human GRCh38 chr11: 77,800,201-77,899,700 , GRCh37.p13 chr11: 77,511,247-77,610,746 INTS4, RSF1, 3 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
    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
    nsv6463048copy number variation1nstd223human GRCh38 chr11: 77,702,166-77,945,031 , GRCh37.p13 chr11: 77,413,211-77,656,077 AAMDC, INTS4, 4 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
    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
    nsv4989066copy number variation1nstd200human GRCh38 chr11: 77,814,098-77,827,051 , GRCh37.p13 chr11: 77,525,144-77,538,097 RSF1, AAMDC, 1 more genes
    nsv4989064copy number variation1nstd200human GRCh38 chr11: 77,702,166-77,945,032 , GRCh37.p13 chr11: 77,413,211-77,656,078 FTH1P16, RSF1, 4 more genes
    nsv4829619copy number variation1nstd200human GRCh37 chr11: 77,525,144-77,538,097 , GRCh38.p12 chr11: 77,814,098-77,827,051 RSF1, AAMDC, 1 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
    nsv4209422copy number variation1nstd166human GRCh37.p13 chr11: 77,413,211-77,656,078 , GRCh38.p12 chr11: 77,702,166-77,945,032 FTH1P16, AAMDC, 4 more genes
    nsv3921121copy number variation1nstd102humanPathogenic GRCh38 chr11: 75,941,754-98,357,960 , NCBI36 chr11: 75,330,446-97,733,898 , GRCh37 chr11: 75,652,798-98,228,688 LOC105369441, RNU6-1135P, 296 more genes
    nsv3915804copy number variation1nstd102humanPathogenic GRCh37 chr11: 71,680,927-77,943,941 , NCBI36 chr11: 71,358,575-77,621,589 , GRCh38 chr11: 71,969,881-78,232,895 TPBGL, MAP6, 173 more genes
    nsv3909688copy number variation1nstd102humanUncertain significance GRCh37 chr11: 76,895,239-77,568,340 , GRCh38.p12 chr11: 77,184,194-77,857,294 AQP11, FTH1P16, 11 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 more genes
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 RTN3, KRTAP5-13P, 2833 more genes
    nsv3898361copy number variation1nstd102humanPathogenic GRCh37 chr11: 71,588,805-116,680,918 , GRCh38.p12 chr11: 71,877,759-116,810,202 SESN3, LOC107984352, 694 more genes
    nsv3894547copy number variation1nstd102humanUncertain significance GRCh37 chr11: 77,415,541-77,785,783 , GRCh38.p12 chr11: 77,704,496-78,074,737 AAMDC, NDUFC2, 8 more genes
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