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Items: 1 to 20 of 73

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5496888copy number variation1nstd206human GRCh38 chr11: 8,676,695-8,681,756 , GRCh37.p13 chr11: 8,698,242-8,703,303 TRIM66, RPL27A
    nsv4978136copy number variation1nstd200human GRCh38 chr11: 8,686,227-8,689,967 , GRCh37.p13 chr11: 8,707,774-8,711,514 RPL27A
    nsv4978135copy number variation1nstd200human GRCh38 chr11: 8,685,968-8,686,092 , GRCh37.p13 chr11: 8,707,515-8,707,639 RPL27A, SNORA3B
    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
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 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
    nsv4381760copy number variation1nstd173human GRCh37 chr11: 8,172,302-9,323,454 , GRCh38.p12 chr11: 8,150,755-9,301,907 , KRT8P41, 26 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
    nsv4204280copy number variation1nstd166human GRCh37.p13 chr11: 8,703,000-8,710,000 , GRCh38.p12 chr11: 8,681,453-8,688,453 TRIM66, SNORA3A, 2 more genes
    nsv3923443copy number variation1nstd102humanUncertain significance NCBI36 chr11: 7,973,799-10,415,328 , GRCh37 chr11: 8,017,223-10,458,752 , GRCh38 chr11: 7,995,676-10,437,205 TMEM41B, AKIP1, 51 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
    nsv3902973copy number variation1nstd102humanPathogenic GRCh37 chr11: 6,969,013-9,257,231 , GRCh38.p12 chr11: 6,947,782-9,235,684 NLRP14, NRIP3, 55 more genes
    nsv3901627copy number variation1nstd102humanUncertain significance GRCh37 chr11: 7,837,338-9,295,428 , GRCh38.p12 chr11: 7,815,791-9,273,881 DENND2B, OR5E1P, 37 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
    nsv3898926copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-37,698,540 , GRCh38.p12 chr11: 230,615-37,676,990 OR51L1, OR52V1P, 771 more genes
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