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Items: 1 to 20 of 133

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7066047inversion1nstd229human GRCh38 chr9: 122,371,847-123,071,176 , GRCh37.p13 chr9: 125,134,126-125,833,455 LOC100422501, OR1H1P, 28 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
    nsv6454208copy number variation1nstd223human GRCh38 chr9: 122,926,058-122,928,068 , GRCh37.p13 chr9: 125,688,337-125,690,347 ZBTB26
    nsv6447100copy number variation1nstd223human GRCh38 chr9: 122,832,501-122,945,100 , GRCh37.p13 chr9: 125,594,780-125,707,379 KRT18P67, ZBTB26, 6 more genes
    nsv6445603copy number variation1nstd223human GRCh38 chr9: 122,897,559-122,919,606 , GRCh37.p13 chr9: 125,659,838-125,681,885 RC3H2, ZBTB6, 1 more genes
    nsv6442918copy number variation1nstd223human GRCh38 chr9: 122,907,749-122,915,271 , GRCh37.p13 chr9: 125,670,028-125,677,550 ZBTB6, ZBTB26
    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
    nsv6240215mobile element insertion1nstd215human GRCh38 chr9: 122,917,562-122,917,562 , GRCh37.p13 chr9: 125,679,841-125,679,841 ZBTB26
    nsv6137055copy number variation2nstd213human GRCh37 chr9: 125,620,000-125,990,001 , GRCh38.p12 chr9: 122,857,721-123,227,722 ZBTB6, MIR600, 11 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
    nsv5970603inversion1nstd209human GRCh38 chr9: 122,761,784-123,114,887 , GRCh37.p13 chr9: 125,524,063-125,877,166 GPR21, PDCL, 16 more genes
    nsv5926108copy number variation1nstd209human GRCh38 chr9: 122,914,268-122,914,838 , GRCh37.p13 chr9: 125,676,547-125,677,117 ZBTB26
    nsv5698144mobile element insertion2nstd211human GRCh38 chr9: 122,917,562-122,917,562 , GRCh37.p13 chr9: 125,679,841-125,679,841 ZBTB26
    nsv5493343copy number variation1nstd206human GRCh38 chr9: 122,914,148-122,914,803 , GRCh37.p13 chr9: 125,676,427-125,677,082 ZBTB26
    nsv5394758mobile element insertion1nstd206human GRCh38 chr9: 122,917,562-122,917,613 , GRCh37.p13 chr9: 125,679,841-125,679,892 ZBTB26
    nsv5373082translocation1nstd200human GRCh38 chr9: 122,914,174-122,914,174 , GRCh38 chr9: 122,914,083-122,914,083 , GRCh37.p13 chr9: 125,676,362-125,676,362 , GRCh37.p13 chr9: 125,676,453-125,676,453 ZBTB26
    nsv5134937mobile element insertion1nstd203human GRCh38 chr9: 122,917,552-122,917,562 , GRCh37.p13 chr9: 125,679,831-125,679,841 ZBTB26
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