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Items: 1 to 20 of 327

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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
    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
    nsv6906811copy number variation1nstd229human GRCh38 chr11: 126,256,035-126,263,960 , GRCh37.p13 chr11: 126,125,930-126,133,855 SRPRA, FAM118B
    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
    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
    nsv6585377inversion1nstd223human GRCh38 chr11: 126,237,128-126,238,153 , GRCh37.p13 chr11: 126,107,023-126,108,048 FAM118B
    nsv6584288inversion1nstd223human GRCh38 chr11: 126,237,239-126,238,213 , GRCh37.p13 chr11: 126,107,134-126,108,108 FAM118B
    nsv6582777inversion1nstd223human GRCh38 chr11: 126,248,012-126,248,388 , GRCh37.p13 chr11: 126,117,907-126,118,283 FAM118B
    nsv6463127copy number variation1nstd223human GRCh38 chr11: 126,214,118-126,216,114 , GRCh37.p13 chr11: 126,084,013-126,086,009 RNU4-86P, FAM118B
    nsv6459395copy number variation1nstd223human GRCh38 chr11: 126,243,416-126,248,386 , GRCh37.p13 chr11: 126,113,311-126,118,281 FAM118B, RN7SL351P
    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
    nsv6309036copy number variation3nstd102humanUncertain significance GRCh37 chr11: 123,504,851-126,163,012 , GRCh38.p12 chr11: 123,634,143-126,293,117 CDON, PKNOX2-DT, 113 more genes
    nsv6304956copy number variation1nstd186human GRCh37 chr11: 126,105,580-126,109,516 , GRCh38.p12 chr11: 126,235,685-126,239,621 FAM118B
    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
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