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Items: 1 to 20 of 178

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5709693mobile element insertion2nstd211human GRCh38 chr13: 102,883,709-102,883,709 , GRCh37.p13 chr13: 103,536,059-103,536,059 METTL21EP
    nsv5672796copy number variation1nstd102humanPathogenic GRCh37 chr13: 94,679,977-111,536,145 , GRCh38.p12 chr13: 94,027,723-110,883,798 LINC00359, LOC107984609, 220 more genes
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5427209mobile element insertion1nstd206human GRCh38 chr13: 102,883,709-102,883,760 , GRCh37.p13 chr13: 103,536,059-103,536,110 METTL21EP
    nsv5159898mobile element insertion1nstd203human GRCh38 chr13: 102,883,695-102,883,709 , GRCh37.p13 chr13: 103,536,045-103,536,059 METTL21EP
    nsv5033445inversion1nstd200human GRCh38 chr13: 63,639,797-112,722,344 , GRCh37.p13 chr13: 64,213,930-113,376,658 , RPL15P18, 564 more genes
    nsv4993929copy number variation1nstd200human GRCh38 chr13: 102,777,238-103,138,970 , GRCh37.p13 chr13: 103,429,588-103,791,320 POGLUT2, RNY5P8, 5 more genes
    nsv4871044inversion1nstd200human GRCh37 chr13: 64,213,930-113,376,658 , GRCh38.p12 chr13: 63,639,797-112,722,344 , TUBGCP3, 564 more genes
    nsv4728419copy number variation1nstd102humanPathogenic GRCh37 chr13: 102,175,801-115,169,858 , GRCh38.p12 chr13: 101,523,450-114,344,403 RPL7P45, LOC107984615, 182 more genes
    nsv4675892copy number variation1nstd102humanPathogenic GRCh37 chr13: 96,240,346-106,103,782 , GRCh38.p12 chr13: 95,588,092-105,451,433 LOC105370328, LINC00554, 132 more genes
    nsv4675850copy number variation1nstd102humanPathogenic GRCh37 chr13: 53,262,013-115,107,733 , GRCh38.p12 chr13: 52,687,878-114,342,258 TEX30, LOC101927712, 680 more genes
    nsv4675791copy number variation1nstd102humanUncertain significance GRCh37 chr13: 103,110,523-103,542,410 , GRCh38.p12 chr13: 102,458,173-102,890,060 LOC107984588, LOC105370337, 10 more genes
    nsv4675644copy number variation1nstd102humanPathogenic GRCh37 chr13: 96,895,656-115,107,733 , GRCh38.p12 chr13: 96,243,402-114,342,258 ZIC2, LINC03032, 266 more genes
    nsv4675610copy number variation1nstd102humanUncertain significance GRCh37 chr13: 102,424,990-104,002,717 , GRCh38.p12 chr13: 101,772,640-103,350,367 POGLUT2, TPP2, 25 more genes
    nsv4571257mobile element insertion1nstd166human GRCh37.p13 chr13: 103,539,469-103,539,469 , GRCh38.p12 chr13: 102,887,119-102,887,119 METTL21EP
    nsv4546102insertion1nstd166human GRCh37.p13 chr13: 103,536,045-103,536,045 , GRCh38.p12 chr13: 102,883,695-102,883,695 METTL21EP
    nsv4500020mobile element insertion1nstd166human GRCh37.p13 chr13: 103,546,348-103,546,348 , GRCh38.p12 chr13: 102,893,998-102,893,998 METTL21EP
    nsv4457315copy number variation1nstd102humanUncertain significance GRCh37 chr13: 103,493,953-104,359,015 , GRCh38.p12 chr13: 102,841,603-103,706,665 SLC10A2, METTL21EP, 7 more genes
    nsv4457251copy number variation1nstd102humanUncertain significance GRCh37 chr13: 103,473,069-104,588,536 , GRCh38.p12 chr13: 102,820,719-103,936,186 LINC01309, ERCC5, 7 more genes
    nsv4456561copy number variation1nstd102humanPathogenic GRCh37 chr13: 61,775,567-115,107,733 , GRCh38.p12 chr13: 61,201,433-114,342,258 LOC105370262, LINC01080, 609 more genes
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