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Items: 1 to 20 of 173

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6870436copy number variation1nstd229human GRCh38 chr9: 122,185,573-122,197,533 , GRCh37.p13 chr9: 124,947,852-124,959,812 LHX6, MORN5
    nsv6866233copy number variation1nstd229human GRCh38 chr9: 122,175,801-122,180,600 , GRCh37.p13 chr9: 124,938,080-124,942,879 MORN5
    nsv6859395copy number variation1nstd229human GRCh38 chr9: 122,186,139-122,196,346 , GRCh37.p13 chr9: 124,948,418-124,958,625 LHX6, MORN5
    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
    nsv6570001inversion1nstd223human GRCh38 chr9: 122,176,776-122,177,577 , GRCh37.p13 chr9: 124,939,055-124,939,856 MORN5
    nsv6442897copy number variation1nstd223human GRCh38 chr9: 122,185,307-122,189,620 , GRCh37.p13 chr9: 124,947,586-124,951,899 LHX6, MORN5
    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
    nsv6187096copy number variation1nstd214human GRCh38 chr9: 122,185,431-122,185,564 , GRCh37.p13 chr9: 124,947,710-124,947,843 MORN5, LHX6
    nsv6187048copy number variation1nstd214human GRCh38 chr9: 122,185,417-122,185,549 , GRCh37.p13 chr9: 124,947,696-124,947,828 LHX6, MORN5
    nsv6176497copy number variation1nstd214human GRCh38 chr9: 122,185,148-122,185,314 , GRCh37.p13 chr9: 124,947,427-124,947,593 LHX6, MORN5
    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
    nsv6014056copy number variation1nstd212human GRCh38 chr9: 122,185,424-122,185,559 , GRCh37.p13 chr9: 124,947,703-124,947,838 MORN5, LHX6
    nsv5924292copy number variation1nstd209human GRCh38 chr9: 122,185,417-122,185,549 , GRCh37.p13 chr9: 124,947,696-124,947,828 LHX6, MORN5
    nsv5640866insertion1nstd207human GRCh38 chr9: 122,191,048-122,191,048 , GRCh37.p13 chr9: 124,953,327-124,953,327 LHX6, MORN5
    nsv5634759insertion1nstd207human GRCh38 chr9: 122,185,417-122,185,417 , GRCh37.p13 chr9: 124,947,696-124,947,696 LHX6, MORN5
    nsv5631269insertion1nstd207human GRCh38 chr9: 122,189,561-122,189,561 , GRCh37.p13 chr9: 124,951,840-124,951,840 LHX6, MORN5
    nsv5604518copy number variation1nstd207human GRCh38 chr9: 122,185,417-122,185,549 , GRCh37.p13 chr9: 124,947,696-124,947,828 LHX6, MORN5
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