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Items: 1 to 20 of 86

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7066313inversion1nstd229human GRCh38 chr11: 6,624,146-15,294,249 , GRCh37.p13 chr11: 6,645,377-15,315,795 RNA5SP332, TMEM41B, 163 more genes
    nsv6906971copy number variation1nstd229human GRCh38 chr11: 6,634,801-9,831,623 , GRCh37.p13 chr11: 6,656,032-9,853,170 RIC3, LOC644656, 86 more genes
    nsv6903616copy number variation1nstd229human GRCh38 chr11: 9,654,101-9,658,900 , GRCh37.p13 chr11: 9,675,648-9,680,447 RPL21P97
    nsv6578417inversion1nstd223human GRCh38 chr11: 7,263,807-16,565,752 , GRCh37.p13 chr11: 7,285,038-16,587,299 TEAD1, IRAG1, 151 more genes
    nsv6449891copy number variation1nstd223human GRCh38 chr11: 9,622,379-10,132,538 , GRCh37.p13 chr11: 9,643,926-10,154,085 SWAP70, LINC02709, 8 more genes
    nsv6444581copy number variation1nstd223human GRCh38 chr11: 9,622,154-10,132,457 , GRCh37.p13 chr11: 9,643,701-10,154,004 RN7SKP50, RPL21P97, 8 more genes
    nsv6442855copy number variation1nstd223human GRCh38 chr11: 6,634,801-9,831,623 , GRCh37.p13 chr11: 6,656,032-9,853,170 LOC105369149, C11orf16, 86 more genes
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv6142995copy number variation1nstd206human GRCh38 chr11: 9,654,000-9,659,500 , GRCh37.p13 chr11: 9,675,547-9,681,047 RPL21P97
    nsv6132292copy number variation1nstd213human GRCh37 chr11: 9,120,000-9,850,001 , GRCh38.p12 chr11: 9,098,453-9,828,454 WEE1, ZNF143, 16 more genes
    nsv5925282copy number variation1nstd209human GRCh38 chr11: 9,623,316-10,133,753 , GRCh37.p13 chr11: 9,644,863-10,155,300 SWAP70, LOC101928008, 8 more genes
    nsv5912011copy number variation1nstd209human GRCh38 chr11: 9,623,387-10,133,591 , GRCh37.p13 chr11: 9,644,934-10,155,138 RN7SKP50, RPL21P97, 8 more genes
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4680411copy number variation1nstd189human GRCh37.p13 chr11: 9,358,141-9,813,308 , GRCh38.p12 chr11: 9,336,594-9,791,761 WEE1, ZNF143, 11 more genes
    nsv4679723copy number variation1nstd189human GRCh37.p13 chr11: 9,647,838-10,160,052 , GRCh38.p12 chr11: 9,626,291-10,138,505 GLULP2, SWAP70, 8 more genes
    nsv4679528copy number variation1nstd189human GRCh37.p13 chr11: 9,640,887-10,164,410 , GRCh38.p12 chr11: 9,619,340-10,142,863 GLULP2, SWAP70, 8 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4616855copy number variation1nstd183human GRCh37 chr11: 9,645,441-10,152,438 , GRCh38.p12 chr11: 9,623,894-10,130,891 SBF2-AS1, RNU7-28P, 8 more genes
    nsv4599100copy number variation1nstd183human GRCh37 chr11: 9,647,837-10,150,593 , GRCh38.p12 chr11: 9,626,290-10,129,046 RPL21P97, RN7SKP50, 8 more genes
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