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Items: 1 to 20 of 148

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5906862copy number variation1nstd209human GRCh38 chr6: 43,197,208-43,197,644 , GRCh37.p13 chr6: 43,164,946-43,165,382 CUL9
    nsv5903446copy number variation1nstd209human GRCh38 chr6: 43,186,570-43,186,766 , GRCh37.p13 chr6: 43,154,308-43,154,504 CUL9
    nsv5684687mobile element insertion2nstd211human GRCh38 chr6: 43,193,980-43,193,980 , GRCh37.p13 chr6: 43,161,718-43,161,718 CUL9
    nsv5673766copy number variation1nstd102humanPathogenic GRCh37 chr6: 42,928,506-43,737,486 , GRCh38.p12 chr6: 42,960,768-43,769,749 SRF, POLR1C, 39 more genes
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5461256copy number variation1nstd206human GRCh38 chr6: 43,197,208-43,197,645 , GRCh37.p13 chr6: 43,164,946-43,165,383 CUL9
    nsv5412805mobile element insertion1nstd206human GRCh38 chr6: 43,193,980-43,194,031 , GRCh37.p13 chr6: 43,161,718-43,161,769 CUL9
    nsv4941137copy number variation1nstd200human GRCh38 chr6: 43,186,571-43,186,767 , GRCh37.p13 chr6: 43,154,309-43,154,505 CUL9
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4756329inversion1nstd199human GRCh37 chr6: 26,745,246-58,149,317 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4735754copy number variation1nstd199human GRCh37 chr6: 26,776,020-58,144,810 , GRCh38.p12 chr6: 26,823,536-61,119,912 , RNU6-250P, 1075 more genes
    nsv4598595copy number variation1nstd183human GRCh37 chr6: 43,173,919-43,174,018 , GRCh38.p12 chr6: 43,206,181-43,206,280 CUL9
    nsv4592683copy number variation1nstd183human GRCh37 chr6: 42,627,455-43,357,404 , GRCh38.p12 chr6: 42,659,717-43,389,666 , PEX6, 36 more genes
    nsv4561602sequence alteration1nstd166human GRCh37.p13 chr6: 43,191,226-43,192,014 , GRCh38.p12 chr6: 43,223,488-43,224,276 DNPH1, CUL9
    nsv4557572mobile element insertion1nstd166human GRCh37.p13 chr6: 43,155,193-43,155,193 , GRCh38.p12 chr6: 43,187,455-43,187,455 CUL9
    nsv4487355mobile element insertion1nstd166human GRCh37.p13 chr6: 43,161,698-43,161,698 , GRCh38.p12 chr6: 43,193,960-43,193,960 CUL9
    nsv4350067copy number variation1nstd102humanPathogenic GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650 HLA-DPB2, CIMIP3, 1001 more genes
    nsv4149004copy number variation1nstd166human GRCh37.p13 chr6: 43,154,309-43,154,505 , GRCh38.p12 chr6: 43,186,571-43,186,767 CUL9
    nsv4146953copy number variation1nstd166human GRCh37.p13 chr6: 43,164,912-43,165,383 , GRCh38.p12 chr6: 43,197,174-43,197,645 CUL9
    nsv4136348copy number variation1nstd166human GRCh37.p13 chr6: 43,176,155-43,177,055 , GRCh38.p12 chr6: 43,208,417-43,209,317 CUL9
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