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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
    nsv7066047inversion1nstd229human GRCh38 chr9: 122,371,847-123,071,176 , GRCh37.p13 chr9: 125,134,126-125,833,455 LOC100422501, OR1H1P, 28 more genes
    nsv6875888copy number variation1nstd229human GRCh38 chr9: 122,390,746-122,584,693 , GRCh37.p13 chr9: 125,153,025-125,346,972 OR1J4, OR1N2, 6 more genes
    nsv6875824copy number variation1nstd229human GRCh38 chr9: 122,521,513-122,611,232 , GRCh37.p13 chr9: 125,283,792-125,373,511 OR1H1P, OR1N2, 4 more genes
    nsv6865237copy number variation1nstd229human GRCh38 chr9: 122,487,483-122,534,834 , GRCh37.p13 chr9: 125,249,762-125,297,113 OR1J2, OR1J4, 1 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
    nsv6633665copy number variation1nstd224human GRCh37 chr9: 125,192,159-125,340,264 , GRCh38.p12 chr9: 122,429,880-122,577,985 OR1J4, OR1J2, 5 more genes
    nsv6451254copy number variation1nstd223human GRCh38 chr9: 122,410,501-122,598,500 , GRCh37.p13 chr9: 125,172,780-125,360,779 OR1J2, OR1N1, 5 more genes
    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
    nsv5488809copy number variation1nstd206human GRCh38 chr9: 122,521,338-122,525,856 , GRCh37.p13 chr9: 125,283,617-125,288,135 OR1J2, OR1N1
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4983547copy number variation1nstd200human GRCh38 chr9: 122,521,338-122,525,856 , GRCh37.p13 chr9: 125,283,617-125,288,135 OR1N1, OR1J2
    nsv4974887copy number variation1nstd200human GRCh38 chr9: 122,410,468-122,598,794 , GRCh37.p13 chr9: 125,172,747-125,361,073 OR1J2, OR1N1, 5 more genes
    nsv4839493copy number variation1nstd200human GRCh37 chr9: 125,283,617-125,288,135 , GRCh38.p12 chr9: 122,521,338-122,525,856 OR1J2, OR1N1
    nsv4728975copy number variation1nstd102humanLikely benign GRCh37 chr9: 125,154,228-125,339,689 , GRCh38.p12 chr9: 122,391,949-122,577,410 PTGS1, OR1J4, 6 more genes
    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
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