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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
    nsv7061857inversion1nstd229human GRCh38 chr11: 126,408,405-126,429,897 , GRCh37.p13 chr11: 126,278,300-126,299,792 KIRREL3, ST3GAL4
    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
    nsv6911682copy number variation1nstd229human GRCh38 chr11: 126,388,392-126,397,461 , GRCh37.p13 chr11: 126,258,287-126,267,356 ST3GAL4
    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
    nsv6904260copy number variation1nstd229human GRCh38 chr11: 126,403,654-126,403,717 , GRCh37.p13 chr11: 126,273,549-126,273,612 ST3GAL4
    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
    nsv6902621copy number variation1nstd229human GRCh38 chr11: 126,395,961-126,397,546 , GRCh37.p13 chr11: 126,265,856-126,267,441 ST3GAL4
    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
    nsv6898260copy number variation1nstd229human GRCh38 chr11: 126,405,394-126,405,776 , GRCh37.p13 chr11: 126,275,289-126,275,671 ST3GAL4
    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
    nsv6472293copy number variation1nstd223human GRCh38 chr11: 126,361,950-126,377,553 , GRCh37.p13 chr11: 126,231,845-126,247,448 ST3GAL4
    nsv6466526copy number variation1nstd223human GRCh38 chr11: 126,395,961-126,397,543 , GRCh37.p13 chr11: 126,265,856-126,267,438 ST3GAL4
    nsv6458412copy number variation1nstd223human GRCh38 chr11: 126,351,963-126,353,696 , GRCh37.p13 chr11: 126,221,858-126,223,591 ST3GAL4, GSEC
    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
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