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Items: 1 to 20 of 96

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094097copy number variation1nstd102humanUncertain significance GRCh37 chr11: 6,625,502-6,662,844 , GRCh38.p12 chr11: 6,604,272-6,641,613 TPP1, ILK, 2 more genes
    nsv7093698copy number variation1nstd102humanUncertain significance GRCh37 chr11: 6,411,829-6,662,844 , GRCh38.p12 chr11: 6,390,599-6,641,613 SMPD1, HPX, 11 more genes
    nsv6917011copy number variation1nstd229human GRCh38 chr11: 2,693,282-9,207,515 , GRCh37.p13 chr11: 2,714,512-9,229,062 LOC105376526, OR51E2, 279 more genes
    nsv6905815copy number variation1nstd229human GRCh38 chr11: 6,608,101-6,615,600 , GRCh37.p13 chr11: 6,629,331-6,636,831 TPP1, ILK, 1 more genes
    nsv6903104copy number variation1nstd229human GRCh38 chr11: 6,545,701-6,661,700 , GRCh37.p13 chr11: 6,566,931-6,682,931 TPP1, DNHD1, 4 more genes
    nsv6899514copy number variation1nstd229human GRCh38 chr11: 6,602,704-6,989,609 , GRCh37.p13 chr11: 6,623,934-7,010,840 RRP8, OR2AG1, 19 more genes
    nsv6637864copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,616-8,250,724 , GRCh38.p12 chr11: 230,616-8,229,177 PNPLA2, OR52H1, 372 more genes
    nsv6449516copy number variation1nstd223human GRCh38 chr11: 6,615,201-6,617,800 , GRCh37.p13 chr11: 6,636,432-6,639,031 TPP1
    nsv6437234copy number variation1nstd223human GRCh38 chr11: 6,602,704-6,989,609 , GRCh37.p13 chr11: 6,623,934-7,010,840 ILK, OR2D2, 19 more genes
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv6308940copy number variation1nstd102humanPathogenic GRCh38 chr11: 6,615,162-6,615,233 , GRCh37 chr11: 6,636,393-6,636,464 TPP1
    nsv6290772copy number variation1nstd102humanUncertain significance GRCh37 chr11: 6,502,523-7,248,333 , GRCh38.p12 chr11: 6,481,293-7,227,102 GVINP2, OR2AG2, 26 more genes
    nsv6132268copy number variation1nstd213human GRCh37 chr11: 6,320,000-6,880,001 , GRCh38.p12 chr11: 6,298,770-6,858,770 APBB1, TPP1, 22 more genes
    nsv5672634copy number variation1nstd102humanPathogenic GRCh37 chr11: 6,559,613-6,640,631 , GRCh38.p12 chr11: 6,538,383-6,619,400 TPP1, ILK, 4 more genes
    nsv4768373copy number variation1nstd102humanPathogenic GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811 LOC107984302, STK33, 375 more genes
    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
    nsv4681173copy number variation2nstd102humanUncertain significance GRCh37 chr11: 5,709,028-6,640,651 , GRCh38.p12 chr11: 5,687,798-6,619,420 OR56B2P, TRIM3, 50 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4456790copy number variation1nstd102humanUncertain significance GRCh37 chr11: 6,607,967-6,796,286 , GRCh38.p12 chr11: 6,586,737-6,775,055 ILK, MRPL17, 8 more genes
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