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Items: 1 to 20 of 153

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5923882copy number variation1nstd209human GRCh38 chr11: 34,117,308-34,140,658 , GRCh37.p13 chr11: 34,138,855-34,162,205 NAT10
    nsv5908879copy number variation1nstd209human GRCh38 chr11: 34,141,327-34,141,398 , GRCh37.p13 chr11: 34,162,874-34,162,945 NAT10
    nsv5865991copy number variation2nstd209human GRCh38 chr11: 34,135,927-34,137,026 , GRCh37.p13 chr11: 34,157,474-34,158,573 NAT10
    nsv5858610copy number variation1nstd209human GRCh38 chr11: 34,131,290-34,132,326 , GRCh37.p13 chr11: 34,152,837-34,153,873 NAT10
    nsv5853873copy number variation1nstd209human GRCh38 chr11: 34,117,288-34,136,376 , GRCh37.p13 chr11: 34,138,835-34,157,923 NAT10
    nsv5851072copy number variation2nstd209human GRCh38 chr11: 34,124,491-34,126,790 , GRCh37.p13 chr11: 34,146,038-34,148,337 NAT10
    nsv5704634mobile element insertion1nstd211human GRCh38 chr11: 34,117,214-34,117,214 , GRCh37.p13 chr11: 34,138,761-34,138,761 NAT10
    nsv5512957copy number variation1nstd206human GRCh38 chr11: 34,104,035-34,104,389 , GRCh37.p13 chr11: 34,125,582-34,125,936 NAT10
    nsv5496621copy number variation1nstd206human GRCh38 chr11: 34,122,300-34,125,426 , GRCh37.p13 chr11: 34,143,847-34,146,973 NAT10
    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
    nsv5354927translocation1nstd200human GRCh38 chr11: 34,104,246-34,104,246 , GRCh38 chr11: 34,104,049-34,104,049 , GRCh37.p13 chr11: 34,125,596-34,125,596 , GRCh37.p13 chr11: 34,125,793-34,125,793 NAT10
    nsv5192111mobile element insertion1nstd203human GRCh38 chr11: 34,143,124-34,143,136 , GRCh37.p13 chr11: 34,164,671-34,164,683 NAT10
    nsv5135723mobile element insertion1nstd203human GRCh38 chr11: 34,132,592-34,132,604 , GRCh37.p13 chr11: 34,154,139-34,154,151 NAT10
    nsv4987022copy number variation1nstd200human GRCh38 chr11: 34,125,965-34,128,297 , GRCh37.p13 chr11: 34,147,512-34,149,844 NAT10
    nsv4984381copy number variation1nstd200human GRCh38 chr11: 34,089,467-34,240,956 , GRCh37.p13 chr11: 34,111,014-34,262,503 , ABTB2, 2 more genes
    nsv4841089copy number variation1nstd200human GRCh37 chr11: 34,111,015-34,262,503 , GRCh38.p12 chr11: 34,089,468-34,240,956 , CAPRIN1, 2 more genes
    nsv4838099copy number variation1nstd200human GRCh37 chr11: 34,138,858-34,162,206 , GRCh38.p12 chr11: 34,117,311-34,140,659 NAT10
    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
    nsv4675518copy number variation1nstd102humanUncertain significance GRCh37 chr11: 33,221,821-34,569,417 , GRCh38.p12 chr11: 33,200,275-34,547,870 HIPK3, C11orf91, 20 more genes
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