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Items: 1 to 20 of 217

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7073885inversion1nstd229human GRCh38 chr9: 121,488,083-121,524,177 , GRCh37.p13 chr9: 124,250,361-124,286,456 RN7SL187P, HMGB1P37, 1 more genes
    nsv6875987copy number variation1nstd229human GRCh38 chr9: 121,466,701-121,506,540 , GRCh37.p13 chr9: 124,228,979-124,268,819 GGTA1, RN7SL187P
    nsv6874552copy number variation1nstd229human GRCh38 chr9: 121,489,855-121,607,569 , GRCh37.p13 chr9: 124,252,133-124,369,848 DAB2IP, HMGB1P37, 3 more genes
    nsv6860580copy number variation1nstd229human GRCh38 chr9: 121,253,488-121,755,032 , GRCh37.p13 chr9: 124,015,766-124,517,311 RN7SL187P, GGTA1, 8 more genes
    nsv6860527copy number variation1nstd229human GRCh38 chr9: 121,448,630-121,453,295 , GRCh37.p13 chr9: 124,210,908-124,215,573 GGTA1
    nsv6860046copy number variation1nstd229human GRCh38 chr9: 121,481,332-121,481,503 , GRCh37.p13 chr9: 124,243,610-124,243,781 GGTA1
    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
    nsv6574696inversion1nstd223human GRCh38 chr9: 121,456,820-121,458,544 , GRCh37.p13 chr9: 124,219,098-124,220,822 GGTA1
    nsv6571317inversion1nstd223human GRCh38 chr9: 121,456,731-121,458,449 , GRCh37.p13 chr9: 124,219,009-124,220,727 GGTA1
    nsv6557051inversion1nstd223human GRCh38 chr9: 121,457,669-121,458,055 , GRCh37.p13 chr9: 124,219,947-124,220,333 GGTA1
    nsv6444230copy number variation1nstd223human GRCh38 chr9: 121,464,625-121,465,540 , GRCh37.p13 chr9: 124,226,903-124,227,818 GGTA1
    nsv6441187copy number variation1nstd223human GRCh38 chr9: 121,487,814-121,491,752 , GRCh37.p13 chr9: 124,250,092-124,254,030 GGTA1
    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
    nsv6174770copy number variation1nstd214human GRCh38 chr9: 121,480,995-121,481,056 , GRCh37.p13 chr9: 124,243,273-124,243,334 GGTA1
    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
    nsv6122639copy number variation1nstd186human GRCh37 chr9: 124,227,009-124,227,390 , GRCh38.p12 chr9: 121,464,731-121,465,112 GGTA1
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