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Items: 1 to 20 of 115

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075743inversion1nstd229human GRCh38 chr9: 120,913,172-120,919,548 , GRCh37.p13 chr9: 123,675,450-123,681,826 TRAF1
    nsv6869795copy number variation1nstd229human GRCh38 chr9: 120,864,301-120,913,700 , GRCh37.p13 chr9: 123,626,579-123,675,978 PHF19, TRAF1
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6447237copy number variation1nstd223human GRCh38 chr9: 120,914,899-120,919,541 , GRCh37.p13 chr9: 123,677,177-123,681,819 TRAF1
    nsv6435917copy number variation1nstd223human GRCh38 chr9: 120,897,175-120,906,917 , GRCh37.p13 chr9: 123,659,453-123,669,195 PHF19, TRAF1
    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
    nsv6290238copy number variation1nstd102humanUncertain significance GRCh37 chr9: 117,853,848-124,633,077 , GRCh38.p12 chr9: 115,091,569-121,870,798 LINC00474, LOC107987123, 72 more genes
    nsv6137053copy number variation1nstd213human GRCh37 chr9: 123,580,000-123,920,001 , GRCh38.p12 chr9: 120,817,722-121,157,723 C5, PSMD5, 5 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
    nsv6092962insertion1nstd212human GRCh38 chr9: 120,924,580-120,924,580 , GRCh37.p13 chr9: 123,686,858-123,686,858 TRAF1
    nsv5909775copy number variation1nstd209human GRCh38 chr9: 120,929,183-120,929,245 , GRCh37.p13 chr9: 123,691,461-123,691,523 TRAF1
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4983499copy number variation1nstd200human GRCh38 chr9: 120,914,899-120,919,541 , GRCh37.p13 chr9: 123,677,177-123,681,819 TRAF1
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 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
    nsv4343265sequence alteration1nstd166human GRCh37.p13 chr9: 123,579,171-124,453,597 , GRCh38.p12 chr9: 120,816,893-121,691,318 C5, GSN, 17 more genes
    nsv4337085sequence alteration1nstd166human GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042 , ABCA1, 927 more genes
    nsv4181851copy number variation1nstd166human GRCh37.p13 chr9: 123,659,453-123,669,199 , GRCh38.p12 chr9: 120,897,175-120,906,921 PHF19, TRAF1
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