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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
    nsv6875159copy number variation1nstd229human GRCh38 chr9: 122,541,346-122,647,699 , GRCh37.p13 chr9: 125,303,625-125,409,978 OR1N2, OR1B1, 4 more genes
    nsv6866563copy number variation1nstd229human GRCh38 chr9: 122,539,558-122,617,925 , GRCh37.p13 chr9: 125,301,837-125,380,204 OR1J2, OR1B1, 4 more genes
    nsv6860966copy number variation1nstd229human GRCh38 chr9: 122,553,726-122,671,205 , GRCh37.p13 chr9: 125,316,005-125,433,484 OR1J2, OR1B1, 5 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
    nsv6455307copy number variation1nstd223human GRCh38 chr9: 122,553,726-122,671,201 , GRCh37.p13 chr9: 125,316,005-125,433,480 OR1L1, OR1J2, 5 more genes
    nsv6437514copy number variation1nstd223human GRCh38 chr9: 122,541,346-122,647,696 , GRCh37.p13 chr9: 125,303,625-125,409,975 OR1H1P, OR1N2, 4 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
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4974889copy number variation1nstd200human GRCh38 chr9: 122,541,346-122,647,699 , GRCh37.p13 chr9: 125,303,625-125,409,978 OR1J2, OR1B1, 4 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
    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
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4457071copy number variation1nstd102humanUncertain significance GRCh37 chr9: 125,349,988-126,462,569 , GRCh38.p12 chr9: 122,587,709-123,700,290 LOC105376265, OR1L1, 30 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
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