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Items: 1 to 20 of 171

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5683088mobile element insertion2nstd211human GRCh38 chr6: 43,927,750-43,927,750 , GRCh37.p13 chr6: 43,895,487-43,895,487 LINC01512
    nsv5638412insertion1nstd207human GRCh38 chr6: 43,927,737-43,927,737 , GRCh37.p13 chr6: 43,895,474-43,895,474 LINC01512
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5400992mobile element insertion1nstd206human GRCh38 chr6: 43,927,737-43,927,737 , GRCh37.p13 chr6: 43,895,474-43,895,474 LINC01512
    nsv5118835mobile element insertion1nstd203human GRCh38 chr6: 43,927,740-43,927,745 , GRCh37.p13 chr6: 43,895,477-43,895,482 LINC01512
    nsv5117768mobile element insertion1nstd203human GRCh38 chr6: 43,927,736-43,927,750 , GRCh37.p13 chr6: 43,895,473-43,895,487 LINC01512
    nsv5115646mobile element insertion1nstd203human GRCh38 chr6: 43,927,742-43,927,750 , GRCh37.p13 chr6: 43,895,479-43,895,487 LINC01512
    nsv5110539mobile element insertion1nstd203human GRCh38 chr6: 43,927,737-43,927,750 , GRCh37.p13 chr6: 43,895,474-43,895,487 LINC01512
    nsv5110316mobile element insertion1nstd203human GRCh38 chr6: 43,927,739-43,927,750 , GRCh37.p13 chr6: 43,895,476-43,895,487 LINC01512
    nsv5106876mobile element insertion1nstd203human GRCh38 chr6: 43,927,741-43,927,750 , GRCh37.p13 chr6: 43,895,478-43,895,487 LINC01512
    nsv5106278mobile element insertion1nstd203human GRCh38 chr6: 43,905,286-43,905,295 , GRCh37.p13 chr6: 43,873,023-43,873,032 , LINC01512
    nsv5100901mobile element insertion1nstd203human GRCh38 chr6: 43,927,744-43,927,744 , GRCh37.p13 chr6: 43,895,481-43,895,481 LINC01512
    nsv4766746insertion1nstd199human GRCh37 chr6: 43,895,482-43,895,482 , GRCh38.p12 chr6: 43,927,745-43,927,745 LINC01512
    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
    nsv4716874mobile element insertion1nstd186human GRCh37 chr6: 43,895,474-43,895,474 , GRCh38.p12 chr6: 43,927,737-43,927,737 LINC01512
    nsv4690418mobile element insertion1nstd186human GRCh37 chr6: 43,895,487-43,895,487 , GRCh38.p12 chr6: 43,927,750-43,927,750 LINC01512
    nsv4484252mobile element insertion1nstd166human GRCh37.p13 chr6: 43,895,474-43,895,474 , GRCh38.p12 chr6: 43,927,737-43,927,737 LINC01512
    nsv4439785insertion1nstd175human GRCh37 chr6: 43,895,474-43,895,474 , GRCh38.p12 chr6: 43,927,737-43,927,737 LINC01512
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