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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv4675144copy number variation1nstd102humanUncertain significance GRCh37 chr11: 6,890,900-6,969,676 , GRCh38.p12 chr11: 6,869,669-6,948,445 OR2D3, OR10A4, 4 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
    nsv4612637copy number variation1nstd183human GRCh37 chr11: 6,932,396-6,956,515 , GRCh38.p12 chr11: 6,911,165-6,935,284 LOC107984019, ZNF215, 1 more genes
    nsv4612281copy number variation1nstd183human GRCh37 chr11: 6,707,887-6,963,165 , GRCh38.p12 chr11: 6,686,656-6,941,934 OR10A2, OR10A4, 12 more genes
    nsv4578256copy number variation1nstd102humanUncertain significance GRCh37 chr11: 6,851,550-6,984,119 , GRCh38.p12 chr11: 6,830,319-6,962,888 OR2D2, OR10A2, 7 more genes
    nsv4565647inversion1nstd166human GRCh37.p13 chr11: 6,776,274-9,026,287 , GRCh38.p12 chr11: 6,755,043-9,004,740 , ZNF215, 61 more genes
    nsv4455989copy number variation1nstd102humanUncertain significance GRCh37 chr11: 6,908,898-7,058,885 , GRCh38.p12 chr11: 6,887,667-7,037,654 ZNF214, OR2D2, 5 more genes
    nsv4455708copy number variation1nstd102humanUncertain significance GRCh37 chr11: 6,754,444-6,982,365 , GRCh38.p12 chr11: 6,733,213-6,961,134 ZNF215, OR10A5, 11 more genes
    nsv4370152copy number variation1nstd173human GRCh37 chr11: 6,629,042-8,085,652 , GRCh38.p12 chr11: 6,607,812-8,064,105 LOC105376533, GVINP2, 48 more genes
    nsv4350476copy number variation1nstd102humanPathogenic GRCh37 chr11: 193,146-12,643,136 , GRCh38.p12 chr11: 193,146-12,621,589 KRTAP5-3, OR56A7P, 457 more genes
    nsv4207692copy number variation1nstd166human GRCh37.p13 chr11: 6,913,275-6,946,268 , GRCh38.p12 chr11: 6,892,044-6,925,037 OR2D2, OR2D3, 2 more genes
    nsv3919565copy number variation1nstd102humanPathogenic GRCh38 chr11: 61,793-10,727,969 , GRCh37 chr11: 61,793-10,749,516 , NCBI36 chr11: 51,793-10,706,092 OR51A7, OR51F5P, 437 more genes
    nsv3912558copy number variation1nstd102humanPathogenic GRCh37 chr11: 446,754-18,926,289 , GRCh38 chr11: 446,754-18,904,742 , NCBI36 chr11: 436,754-18,882,865 TRIM22, CSNK2A3, 546 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 more genes
    nsv3906221copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-31,995,219 , GRCh38.p12 chr11: 230,615-31,973,673 PCNAP4, LIN7C, 688 more genes
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 RTN3, KRTAP5-13P, 2833 more genes
    nsv3898948copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-17,099,213 , GRCh38.p12 chr11: 230,615-17,077,666 MTND5P21, IFITM1, 506 more genes
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