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Items: 1 to 20 of 197

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5638336insertion1nstd207human GRCh38 chr6: 44,391,076-44,391,076 , GRCh37.p13 chr6: 44,358,813-44,358,813 CDC5L
    nsv5629178insertion1nstd207human GRCh38 chr6: 44,411,637-44,411,637 , GRCh37.p13 chr6: 44,379,374-44,379,374 CDC5L
    nsv5565671copy number variation1nstd207human GRCh38 chr6: 44,391,027-44,391,088 , GRCh37.p13 chr6: 44,358,764-44,358,825 CDC5L
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5468305copy number variation1nstd206human GRCh38 chr6: 44,443,996-44,444,046 , GRCh37.p13 chr6: 44,411,733-44,411,783 CDC5L
    nsv5455577copy number variation1nstd206human GRCh38 chr6: 44,394,645-44,394,749 , GRCh37.p13 chr6: 44,362,382-44,362,486 CDC5L
    nsv5196668mobile element insertion1nstd203human GRCh38 chr6: 44,427,126-44,427,138 , GRCh37.p13 chr6: 44,394,863-44,394,875 CDC5L
    nsv5102294mobile element insertion1nstd203human GRCh38 chr6: 44,405,905-44,405,919 , GRCh37.p13 chr6: 44,373,642-44,373,656 CDC5L
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4757340insertion1nstd199human GRCh37 chr6: 44,358,643-44,358,643 , GRCh38.p12 chr6: 44,390,906-44,390,906 CDC5L
    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
    nsv4598599copy number variation1nstd183human GRCh37 chr6: 44,393,909-44,394,056 , GRCh38.p12 chr6: 44,426,172-44,426,319 CDC5L
    nsv4568284mobile element insertion1nstd166human GRCh37.p13 chr6: 44,397,129-44,397,129 , GRCh38.p12 chr6: 44,429,392-44,429,392 CDC5L
    nsv4564807mobile element insertion1nstd166human GRCh37.p13 chr6: 44,359,999-44,359,999 , GRCh38.p12 chr6: 44,392,262-44,392,262 CDC5L
    nsv4523469copy number variation1nstd166human GRCh37.p13 chr6: 44,358,876-44,358,950 , GRCh38.p12 chr6: 44,391,139-44,391,213 CDC5L
    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
    nsv4149368copy number variation1nstd166human GRCh37.p13 chr6: 44,411,733-44,411,783 , GRCh38.p12 chr6: 44,443,996-44,444,046 CDC5L
    nsv4138303copy number variation1nstd166human GRCh37.p13 chr6: 44,362,382-44,362,486 , GRCh38.p12 chr6: 44,394,645-44,394,749 CDC5L
    nsv3949445copy number variation1nstd167human GRCh37 chr6: 44,358,643-44,358,707 , GRCh38.p12 chr6: 44,390,906-44,390,970 CDC5L
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