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Items: 1 to 20 of 146

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146739insertion1nstd232human GRCh37.p13 chr9: 124,906,656-124,906,656 , GRCh38.p12 chr9: 122,144,377-122,144,377 NDUFA8
    nsv6868384copy number variation1nstd229human GRCh38 chr9: 122,150,744-122,154,275 , GRCh37.p13 chr9: 124,913,023-124,916,554 NDUFA8
    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
    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
    nsv5711755mobile element insertion2nstd211human GRCh38 chr9: 122,145,508-122,145,508 , GRCh37.p13 chr9: 124,907,787-124,907,787 NDUFA8
    nsv5409058mobile element insertion1nstd206human GRCh38 chr9: 122,145,508-122,145,559 , GRCh37.p13 chr9: 124,907,787-124,907,838 NDUFA8
    nsv5134388mobile element insertion1nstd203human GRCh38 chr9: 122,145,493-122,145,508 , GRCh37.p13 chr9: 124,907,772-124,907,787 NDUFA8
    nsv5120596mobile element insertion1nstd203human GRCh38 chr9: 122,152,157-122,152,172 , GRCh37.p13 chr9: 124,914,436-124,914,451 NDUFA8
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4983540copy number variation1nstd200human GRCh38 chr9: 122,158,662-122,158,771 , GRCh37.p13 chr9: 124,920,941-124,921,050 NDUFA8, MORN5
    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
    nsv4615662copy number variation1nstd183human GRCh37 chr9: 124,886,752-124,918,150 , GRCh38.p12 chr9: 122,124,473-122,155,871 NDUFA8
    nsv4604110copy number variation1nstd183human GRCh37 chr9: 124,888,993-124,918,180 , GRCh38.p12 chr9: 122,126,714-122,155,901 NDUFA8
    nsv4598981copy number variation1nstd183human GRCh37 chr9: 124,874,636-124,901,377 , GRCh38.p12 chr9: 122,112,357-122,139,098 NDUFA8, MIR4478
    nsv4494994mobile element insertion1nstd166human GRCh37.p13 chr9: 124,907,772-124,907,772 , GRCh38.p12 chr9: 122,145,493-122,145,493 NDUFA8
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
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