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Items: 1 to 20 of 202

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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
    nsv7070443inversion1nstd229human GRCh38 chr11: 125,887,512-126,792,902 , GRCh37.p13 chr11: 125,757,407-126,662,797 CDON, TIRAP, 21 more genes
    nsv6915579copy number variation1nstd229human GRCh38 chr11: 126,310,989-126,341,165 , GRCh37.p13 chr11: 126,180,884-126,211,060 GSEC, DCPS
    nsv6914370copy number variation1nstd229human GRCh38 chr11: 126,276,201-126,567,700 , GRCh37.p13 chr11: 126,146,096-126,437,595 GSEC, TIRAP, 6 more genes
    nsv6909227copy number variation1nstd229human GRCh38 chr11: 126,060,101-126,613,900 , GRCh37.p13 chr11: 125,929,996-126,483,795 RPUSD4, TIRAP-AS1, 15 more genes
    nsv6903691copy number variation1nstd229human GRCh38 chr11: 126,034,501-126,613,900 , GRCh37.p13 chr11: 125,904,396-126,483,795 GSEC, SRPRA, 15 more genes
    nsv6899723copy number variation1nstd229human GRCh38 chr11: 126,208,996-126,563,956 , GRCh37.p13 chr11: 126,078,891-126,433,851 KIRREL3, ST3GAL4, 11 more genes
    nsv6899583copy number variation1nstd229human GRCh38 chr11: 126,310,980-126,545,530 , GRCh37.p13 chr11: 126,180,875-126,415,425 ST3GAL4, DCPS, 2 more genes
    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
    nsv6637236copy number variation1nstd102humanUncertain significance GRCh37 chr11: 125,812,020-126,308,722 , GRCh38.p12 chr11: 125,942,125-126,438,827 RPL35AP26, RNU4-86P, 16 more genes
    nsv6637187copy number variation1nstd102humanUncertain significance GRCh37 chr11: 126,100,551-126,437,941 , GRCh38.p12 chr11: 126,230,656-126,568,046 RN7SL351P, TIRAP, 9 more genes
    nsv6620952copy number variation1nstd224human GRCh37 chr11: 126,162,468-126,215,482 , GRCh38.p12 chr11: 126,292,573-126,345,587 DCPS, GSEC, 2 more genes
    nsv6458412copy number variation1nstd223human GRCh38 chr11: 126,351,963-126,353,696 , GRCh37.p13 chr11: 126,221,858-126,223,591 ST3GAL4, GSEC
    nsv6457088copy number variation1nstd223human GRCh38 chr11: 126,347,381-126,352,432 , GRCh37.p13 chr11: 126,217,276-126,222,327 GSEC, DCPS
    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
    nsv6291074copy number variation1nstd102humanPathogenic GRCh37 chr11: 112,375,478-128,785,742 , GRCh38.p12 chr11: 112,504,755-128,915,847 ZW10, MPZL2, 378 more genes
    nsv6289927copy number variation1nstd102humanPathogenic GRCh37 chr11: 104,288,964-134,937,416 , GRCh38.p12 chr11: 104,418,236-135,067,522 IGSF9B, MIR10526, 592 more genes
    nsv6132348copy number variation1nstd213human GRCh37 chr11: 126,170,000-126,260,001 , GRCh38.p12 chr11: 126,300,105-126,390,106 ST3GAL4, DCPS, 1 more genes
    nsv6132082copy number variation1nstd213human GRCh37 chr11: 126,220,000-126,870,001 , GRCh38.p12 chr11: 126,350,105-127,000,105 MIR3167, KIRREL3-AS2, 8 more genes
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