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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7071535inversion1nstd229human GRCh38 chr9: 124,246,999-128,875,010 , GRCh37.p13 chr9: 127,009,278-131,637,289 PTGES2-AS1, STXBP1, 130 more genes
    nsv7058624inversion1nstd229human GRCh38 chr9: 124,638,888-125,009,541 , GRCh37.p13 chr9: 127,401,167-127,771,820 MIR181A2HG, OLFML2A, 11 more genes
    nsv6870485copy number variation1nstd229human GRCh38 chr9: 124,677,301-124,684,300 , GRCh37.p13 chr9: 127,439,580-127,446,579 NR6A1, MIR181A2HG
    nsv6866308copy number variation1nstd229human GRCh38 chr9: 124,613,446-124,668,570 , GRCh37.p13 chr9: 127,375,725-127,430,849 NR6A1, MIR181A2HG
    nsv6861399copy number variation1nstd229human GRCh38 chr9: 124,691,659-124,703,694 , GRCh37.p13 chr9: 127,453,938-127,465,973 MIR181B2, NR6A1, 2 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
    nsv6563397inversion1nstd223human GRCh38 chr9: 124,665,008-124,666,292 , GRCh37.p13 chr9: 127,427,287-127,428,571 MIR181A2HG, NR6A1
    nsv6560177inversion1nstd223human GRCh38 chr9: 124,687,126-124,688,274 , GRCh37.p13 chr9: 127,449,405-127,450,553 MIR181A2HG, NR6A1
    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
    nsv6137443copy number variation1nstd213human GRCh37 chr9: 126,390,000-129,240,001 , GRCh38.p12 chr9: 123,627,721-126,477,722 NR6A1, GOLGA1, 52 more genes
    nsv6011301copy number variation1nstd212human GRCh38 chr9: 124,670,436-124,670,524 , GRCh37.p13 chr9: 127,432,715-127,432,803 MIR181A2HG, NR6A1
    nsv6006230copy number variation1nstd212human GRCh38 chr9: 124,683,195-124,683,340 , GRCh37.p13 chr9: 127,445,474-127,445,619 NR6A1, MIR181A2HG
    nsv5633042insertion1nstd207human GRCh38 chr9: 124,670,520-124,670,520 , GRCh37.p13 chr9: 127,432,799-127,432,799 NR6A1, MIR181A2HG
    nsv5553002insertion1nstd206human GRCh38 chr9: 124,670,518-124,670,526 , GRCh37.p13 chr9: 127,432,797-127,432,805 NR6A1, MIR181A2HG
    nsv5490563copy number variation1nstd206human GRCh38 chr9: 124,683,198-124,683,339 , GRCh37.p13 chr9: 127,445,477-127,445,618 NR6A1, MIR181A2HG
    nsv5474498copy number variation1nstd206human GRCh38 chr9: 124,670,437-124,670,524 , GRCh37.p13 chr9: 127,432,716-127,432,803 NR6A1, MIR181A2HG
    nsv5379512translocation1nstd200human GRCh38 chr9: 124,677,486-124,677,486 , GRCh38 chr9: 124,679,195-124,679,195 , GRCh37.p13 chr9: 127,439,765-127,439,765 , GRCh37.p13 chr9: 127,441,474-127,441,474 NR6A1, MIR181A2HG
    nsv5373096translocation1nstd200human GRCh38 chr9: 124,680,291-124,680,291 , GRCh38 chr9: 124,677,495-124,677,495 , GRCh37.p13 chr9: 127,442,570-127,442,570 , GRCh37.p13 chr9: 127,439,774-127,439,774 MIR181A2HG, NR6A1
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