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Items: 1 to 20 of 209

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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
    nsv6915524copy number variation1nstd229human GRCh38 chr11: 126,267,799-126,267,920 , GRCh37.p13 chr11: 126,137,694-126,137,815 SRPRA, FOXRED1
    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
    nsv6910636copy number variation1nstd229human GRCh38 chr11: 126,278,313-126,280,200 , GRCh37.p13 chr11: 126,148,208-126,150,095 FOXRED1, RPL35AP26
    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
    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
    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
    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
    nsv6085385insertion1nstd212human GRCh38 chr11: 126,276,315-126,276,315 , GRCh37.p13 chr11: 126,146,210-126,146,210 FOXRED1, RPL35AP26
    nsv5647743insertion1nstd207human GRCh38 chr11: 126,276,308-126,276,308 , GRCh37.p13 chr11: 126,146,203-126,146,203 FOXRED1, RPL35AP26
    nsv4750342insertion1nstd199human GRCh37 chr11: 126,146,199-126,146,199 , GRCh38.p12 chr11: 126,276,304-126,276,304 FOXRED1, RPL35AP26
    nsv4732750copy number variation1nstd199human GRCh37 chr11: 114,433,314-131,230,467 , GRCh38.p12 chr11: 114,562,592-131,360,572 , LINC02702, 392 more genes
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