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Items: 1 to 20 of 113

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5920481copy number variation1nstd209human GRCh38 chr11: 102,449,463-102,546,319 , GRCh37.p13 chr11: 102,320,194-102,417,050 TMEM123-DT, MMP7, 2 more genes
    nsv5856057copy number variation1nstd209human GRCh38 chr11: 102,523,355-102,545,855 , GRCh37.p13 chr11: 102,394,086-102,416,586 MMP7
    nsv5850672copy number variation1nstd209human GRCh38 chr11: 102,449,445-102,521,529 , GRCh37.p13 chr11: 102,320,176-102,392,260 MMP7, LOC102723838, 2 more genes
    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
    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
    nsv5130842mobile element insertion1nstd203human GRCh38 chr11: 102,529,794-102,529,810 , GRCh37.p13 chr11: 102,400,525-102,400,541 MMP7
    nsv5124273mobile element insertion1nstd203human GRCh38 chr11: 102,523,620-102,523,634 , GRCh37.p13 chr11: 102,394,351-102,394,365 MMP7
    nsv4989243copy number variation1nstd200human GRCh38 chr11: 102,449,463-102,546,323 , GRCh37.p13 chr11: 102,320,194-102,417,054 LOC102723838, MMP7, 2 more genes
    nsv4711184copy number variation1nstd195human GRCh37 chr11: 102,376,301-102,612,301 , GRCh38.p12 chr11: 102,505,570-102,741,570 MMP7, MMP8, 3 more genes
    nsv4680427copy number variation1nstd189human GRCh37.p13 chr11: 102,292,343-102,417,253 , GRCh38.p12 chr11: 102,421,612-102,546,522 MMP7, TMEM123, 2 more genes
    nsv4541484insertion1nstd166human GRCh37.p13 chr11: 102,394,351-102,394,351 , GRCh38.p12 chr11: 102,523,620-102,523,620 MMP7
    nsv4198278copy number variation1nstd166human GRCh37.p13 chr11: 102,320,200-102,417,054 , GRCh38.p12 chr11: 102,449,469-102,546,323 MMP7, TMEM123-DT, 2 more genes
    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
    nsv3922508copy number variation1nstd102humanPathogenic GRCh38 chr11: 85,242,847-102,920,097 , GRCh37 chr11: 84,953,891-102,738,968 , NCBI36 chr11: 84,631,539-102,296,037 AMOTL1, LNCRNA-IUR, 240 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
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