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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5711072mobile element insertion2nstd211human GRCh38 chr11: 102,952,312-102,952,312 , GRCh37.p13 chr11: 102,823,041-102,823,041 MMP13
    nsv5672640copy number variation1nstd102humanPathogenic GRCh37 chr11: 94,153,285-111,965,700 , GRCh38.p12 chr11: 94,420,119-112,094,976 HSPD1P13, CARD17P, 239 more genes
    nsv5398867mobile element insertion1nstd206human GRCh38 chr11: 102,952,312-102,952,363 , GRCh37.p13 chr11: 102,823,041-102,823,092 MMP13
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv4989245copy number variation1nstd200human GRCh38 chr11: 102,948,543-102,956,667 , GRCh37.p13 chr11: 102,822,937-102,827,396 MMP13
    nsv4713977copy number variation1nstd195human GRCh37 chr11: 102,690,451-102,909,551 , GRCh38.p12 chr11: 102,819,720-103,038,822 MMP3, MMP12, 4 more genes
    nsv4600864copy number variation1nstd183human GRCh37 chr11: 102,824,739-102,825,140 , GRCh38.p12 chr11: 102,954,010-102,954,411 MMP13
    nsv4544651insertion1nstd166human GRCh37.p13 chr11: 102,814,847-102,814,847 , GRCh38.p12 chr11: 102,944,118-102,944,118 MMP13
    nsv4501565mobile element insertion1nstd166human GRCh37.p13 chr11: 102,823,027-102,823,027 , GRCh38.p12 chr11: 102,952,298-102,952,298 MMP13
    nsv4377422copy number variation1nstd173human GRCh37 chr11: 102,814,716-102,847,882 , GRCh38.p12 chr11: 102,943,987-102,977,153 MMP13
    nsv3924464copy number variation1nstd102humanPathogenic NCBI36 chr11: 97,733,839-105,435,083 , GRCh38 chr11: 98,357,901-106,059,146 , GRCh37 chr11: 98,228,629-105,929,873 ARHGAP42, PDGFDDN, 91 more genes
    nsv3922253copy number variation1nstd102humanPathogenic GRCh37 chr11: 100,219,331-134,910,140 , NCBI36 chr11: 99,724,541-134,415,350 , GRCh38 chr11: 100,348,599-135,040,246 RPS27P19, UBASH3B, 655 more genes
    nsv3915056copy number variation1nstd102humanPathogenic GRCh37 chr11: 101,323,715-103,914,833 , NCBI36 chr11: 100,828,925-103,420,043 , GRCh38 chr11: 101,452,984-104,044,105 MMP27, MMP12, 47 more genes
    nsv3913977copy number variation1nstd102humanPathogenic GRCh37 chr11: 77,943,882-106,650,146 , GRCh38 chr11: 78,232,836-106,779,420 , NCBI36 chr11: 77,621,530-106,155,356 PLS1P1, SNORA25, 349 more genes
    nsv3910663copy number variation1nstd102humanPathogenic GRCh38 chr11: 91,086,659-109,595,582 , NCBI36 chr11: 90,459,475-108,971,518 , GRCh37 chr11: 90,819,827-109,466,308 LOC101060084, PGAM1P9, 230 more genes
    nsv3910101copy number variation1nstd102humanPathogenic NCBI36 chr11: 87,796,211-113,996,548 , GRCh37.p13 chr11: 88,156,563-114,491,338 , GRCh38.p12 chr11: 88,423,395-114,620,616 PHB1P16, LOC100418884, 385 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
    nsv3908142copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 102,578,709-107,230,611 , GRCh38.p12 chr11: 102,707,978-107,359,885 CASP1, CASP4, 65 more genes
    nsv3904761copy number variation1nstd102humanPathogenic GRCh37 chr11: 80,053,454-113,316,236 , GRCh38.p12 chr11: 80,342,410-113,445,514 RPS6P16, CTSC, 449 more genes
    nsv3901935copy number variation1nstd102humanUncertain significance GRCh37 chr11: 102,642,841-102,826,187 , GRCh38.p12 chr11: 102,772,110-102,955,458 MMP3, MMP12, 7 more genes
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