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Items: 1 to 20 of 125

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077833inversion1nstd229human GRCh38 chr9: 122,408,687-122,761,791 , GRCh37.p13 chr9: 125,170,966-125,524,070 OR1J4, OR1J2, 13 more genes
    nsv7072892inversion1nstd229human GRCh38 chr9: 122,723,879-122,725,220 , GRCh37.p13 chr9: 125,486,158-125,487,499 OR1L4
    nsv7066047inversion1nstd229human GRCh38 chr9: 122,371,847-123,071,176 , GRCh37.p13 chr9: 125,134,126-125,833,455 LOC100422501, OR1H1P, 28 more genes
    nsv7059933inversion1nstd229human GRCh38 chr9: 122,719,970-122,724,007 , GRCh37.p13 chr9: 125,482,249-125,486,286 OR1L4
    nsv6876591copy number variation1nstd229human GRCh38 chr9: 122,719,564-122,783,006 , GRCh37.p13 chr9: 125,481,843-125,545,285 SKA2P1, OR1L6, 1 more genes
    nsv6873307copy number variation1nstd229human GRCh38 chr9: 122,723,448-122,723,880 , GRCh37.p13 chr9: 125,485,727-125,486,159 OR1L4
    nsv6869104copy number variation1nstd229human GRCh38 chr9: 122,723,801-122,726,500 , GRCh37.p13 chr9: 125,486,080-125,488,779 OR1L4
    nsv6864280copy number variation1nstd229human GRCh38 chr9: 122,709,651-122,732,250 , GRCh37.p13 chr9: 125,471,930-125,494,529 OR1L4
    nsv6860097copy number variation1nstd229human GRCh38 chr9: 122,668,116-122,879,390 , GRCh37.p13 chr9: 125,430,395-125,641,669 OR1L3, SKA2P1, 9 more genes
    nsv6637981copy number variation1nstd102humanPathogenic GRCh37 chr9: 124,018,736-129,995,568 , GRCh38.p12 chr9: 121,256,458-127,233,289 PBX3-DT, ADGRD2, 119 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6633341copy number variation1nstd224human GRCh37 chr9: 125,486,270-125,542,199 , GRCh38.p12 chr9: 122,723,991-122,779,920 SKA2P1, OR1L4, 1 more genes
    nsv6574419inversion1nstd223human GRCh38 chr9: 122,723,879-122,725,220 , GRCh37.p13 chr9: 125,486,158-125,487,499 OR1L4
    nsv6455235copy number variation1nstd223human GRCh38 chr9: 122,709,635-122,732,248 , GRCh37.p13 chr9: 125,471,914-125,494,527 OR1L4
    nsv6447888copy number variation1nstd223human GRCh38 chr9: 122,724,688-122,750,547 , GRCh37.p13 chr9: 125,486,967-125,512,826 OR1L6, OR1L4
    nsv6447595copy number variation1nstd223human GRCh38 chr9: 122,724,804-122,750,662 , GRCh37.p13 chr9: 125,487,083-125,512,941 OR1L6, OR1L4
    nsv6314001copy number variation1nstd102humanPathogenic GRCh37 chr9: 116,422,275-131,713,233 , GRCh38.p12 chr9: 113,659,995-128,950,954 LOC105376244, RN7SL187P, 286 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6291398copy number variation1nstd102humanPathogenic GRCh37 chr9: 120,045,175-127,335,905 , GRCh38.p12 chr9: 117,282,896-124,573,626 ZBTB6, LOC105376253, 107 more genes
    nsv6137052copy number variation1nstd213human GRCh37 chr9: 123,200,000-125,840,001 , GRCh38.p12 chr9: 120,437,722-123,077,722 MEGF9, GGTA1, 61 more genes
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