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Items: 1 to 20 of 105

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980035inversion1nstd209human GRCh38 chr9: 122,725,223-122,726,567 , GRCh37.p13 chr9: 125,487,502-125,488,846 OR1L4
    nsv5635187insertion1nstd207human GRCh38 chr9: 122,723,878-122,723,878 , GRCh37.p13 chr9: 125,486,157-125,486,157 OR1L4
    nsv5561926mobile element insertion1nstd206human GRCh38 chr9: 122,723,878-122,723,878 , GRCh37.p13 chr9: 125,486,157-125,486,157 OR1L4
    nsv5379509translocation1nstd200human GRCh38 chr9: 122,723,881-122,723,881 , GRCh38 chr9: 122,725,567-122,725,567 , GRCh37.p13 chr9: 125,487,846-125,487,846 , GRCh37.p13 chr9: 125,486,160-125,486,160 OR1L4
    nsv5379508translocation1nstd200human GRCh38 chr9: 122,723,879-122,723,879 , GRCh38 chr9: 122,725,220-122,725,220 , GRCh37.p13 chr9: 125,486,158-125,486,158 , GRCh37.p13 chr9: 125,487,499-125,487,499 OR1L4
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4983555copy number variation1nstd200human GRCh38 chr9: 122,709,634-122,732,251 , GRCh37.p13 chr9: 125,471,913-125,494,530 OR1L4
    nsv4983553copy number variation1nstd200human GRCh38 chr9: 122,702,027-122,787,320 , GRCh37.p13 chr9: 125,464,306-125,549,599 OR5C1, OR1L4, 2 more genes
    nsv4974891copy number variation1nstd200human GRCh38 chr9: 122,724,744-122,750,814 , GRCh37.p13 chr9: 125,487,023-125,513,093 OR1L6, OR1L4
    nsv4836444copy number variation1nstd200human GRCh37 chr9: 125,471,914-125,494,529 , GRCh38.p12 chr9: 122,709,635-122,732,250 OR1L4
    nsv4724673mobile element insertion1nstd186human GRCh37 chr9: 125,486,160-125,486,160 , GRCh38.p12 chr9: 122,723,881-122,723,881 OR1L4
    nsv4676065copy number variation1nstd102humanUncertain significance GRCh37 chr9: 125,105,375-125,616,987 , GRCh38.p12 chr9: 122,343,096-122,854,708 OR1L3, OR1N1, 19 more genes
    nsv4675789copy number variation1nstd102humanUncertain significance GRCh37 chr9: 124,604,592-126,306,080 , GRCh38.p12 chr9: 121,842,313-123,543,801 MIR7150, OR1N2, 43 more genes
    nsv4614741copy number variation1nstd183human GRCh37 chr9: 125,487,286-125,507,460 , GRCh38.p12 chr9: 122,725,007-122,745,181 OR1L4
    nsv4605579copy number variation1nstd183human GRCh37 chr9: 125,478,327-125,492,393 , GRCh38.p12 chr9: 122,716,048-122,730,114 OR1L4
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4457071copy number variation1nstd102humanUncertain significance GRCh37 chr9: 125,349,988-126,462,569 , GRCh38.p12 chr9: 122,587,709-123,700,290 LOC105376265, OR1L1, 30 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
    nsv4425055copy number variation1nstd174human GRCh37 chr9: 125,486,953-125,514,075 , GRCh38.p12 chr9: 122,724,674-122,751,796 OR1L4, OR1L6
    nsv4337085sequence alteration1nstd166human GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042 , ABCA1, 927 more genes
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