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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6128660insertion1nstd186human GRCh37 chr11: 102,590,146-102,590,154 , GRCh38.p12 chr11: 102,719,415-102,719,423 MMP8
    nsv5979883insertion1nstd209human GRCh38 chr11: 102,719,416-102,719,416 , GRCh37.p13 chr11: 102,590,147-102,590,147 MMP8
    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
    nsv5654745insertion1nstd207human GRCh38 chr11: 102,719,415-102,719,415 , GRCh37.p13 chr11: 102,590,146-102,590,146 MMP8
    nsv5554490sequence alteration1nstd206human GRCh38 chr11: 102,719,356-102,720,722 , GRCh37.p13 chr11: 102,590,087-102,591,453 MMP8
    nsv5544489insertion1nstd206human GRCh38 chr11: 102,719,415-102,719,423 , GRCh37.p13 chr11: 102,590,146-102,590,154 MMP8
    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
    nsv4980350copy number variation1nstd200human GRCh38 chr11: 102,714,812-102,716,113 , GRCh37.p13 chr11: 102,585,543-102,586,844 MMP8
    nsv4849048copy number variation1nstd200human GRCh37 chr11: 102,569,934-102,586,355 , GRCh38.p12 chr11: 102,699,203-102,715,624 MMP27, MMP8
    nsv4835663copy number variation1nstd200human GRCh37 chr11: 102,585,564-102,586,817 , GRCh38.p12 chr11: 102,714,833-102,716,086 MMP8
    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
    nsv4611791copy number variation2nstd183human GRCh37 chr11: 102,584,248-102,584,515 , GRCh38.p12 chr11: 102,713,517-102,713,784 MMP8
    nsv4604706copy number variation1nstd183human GRCh37 chr11: 102,583,657-102,584,515 , GRCh38.p12 chr11: 102,712,926-102,713,784 MMP8
    nsv4566112sequence alteration1nstd166human GRCh37.p13 chr11: 102,590,142-102,591,441 , GRCh38.p12 chr11: 102,719,411-102,720,710 MMP8
    nsv4548822insertion1nstd166human GRCh37.p13 chr11: 102,590,146-102,590,146 , GRCh38.p12 chr11: 102,719,415-102,719,415 MMP8
    nsv4511451mobile element insertion1nstd166human GRCh37.p13 chr11: 102,583,092-102,583,092 , GRCh38.p12 chr11: 102,712,361-102,712,361 MMP8
    nsv4209122copy number variation1nstd166human GRCh37.p13 chr11: 102,582,151-102,582,311 , GRCh38.p12 chr11: 102,711,420-102,711,580 MMP8
    nsv4196132copy number variation1nstd166human GRCh37.p13 chr11: 102,593,601-102,596,990 , GRCh38.p12 chr11: 102,722,870-102,726,259 MMP8
    nsv4195671copy number variation1nstd166human GRCh37.p13 chr11: 102,569,935-102,586,355 , GRCh38.p12 chr11: 102,699,204-102,715,624 MMP27, MMP8
    nsv3962548insertion1nstd168human GRCh38 chr11: 102,700,540-102,745,926 , GRCh37.p13 chr11: 102,571,271-102,616,657 MMP8, MMP27
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