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Items: 1 to 20 of 85

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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
    nsv6860097copy number variation1nstd229human GRCh38 chr9: 122,668,116-122,879,390 , GRCh37.p13 chr9: 125,430,395-125,641,669 OR1L3, SKA2P1, 9 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
    nsv6575447inversion1nstd223human GRCh38 chr9: 122,878,851-122,879,126 , GRCh37.p13 chr9: 125,641,130-125,641,405 SNORD90, RC3H2
    nsv6571932inversion1nstd223human GRCh38 chr9: 122,878,736-122,879,265 , GRCh37.p13 chr9: 125,641,015-125,641,544 RC3H2, SNORD90
    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
    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
    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
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 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
    nsv4456842copy number variation1nstd102humanUncertain significance GRCh37 chr9: 125,635,604-125,892,381 , GRCh38.p12 chr9: 122,873,325-123,130,102 LOC100422501, RNY1P15, 11 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
    nsv4337085sequence alteration1nstd166human GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042 , ABCA1, 927 more genes
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