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Items: 1 to 20 of 138

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5899241copy number variation1nstd209human GRCh38 chr6: 42,936,096-42,936,171 , GRCh37.p13 chr6: 42,903,834-42,903,909 CNPY3-GNMT, CNPY3
    nsv5730728mobile element insertion2nstd211human GRCh38 chr6: 42,927,040-42,927,040 , GRCh37.p13 chr6: 42,894,778-42,894,778 CNPY3
    nsv5682503mobile element insertion2nstd211human GRCh38 chr6: 42,935,953-42,935,953 , GRCh37.p13 chr6: 42,903,691-42,903,691 CNPY3, CNPY3-GNMT
    nsv5630250insertion1nstd207human GRCh38 chr6: 42,936,096-42,936,096 , GRCh37.p13 chr6: 42,903,834-42,903,834 CNPY3, CNPY3-GNMT
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5554213mobile element insertion1nstd206human GRCh38 chr6: 42,927,040-42,927,045 , GRCh37.p13 chr6: 42,894,778-42,894,783 CNPY3
    nsv5409411mobile element insertion1nstd206human GRCh38 chr6: 42,935,953-42,936,004 , GRCh37.p13 chr6: 42,903,691-42,903,742 CNPY3-GNMT, CNPY3
    nsv5224950copy number variation1nstd204human GRCh38.p13 chr6: 42,543,301-43,041,600 , GRCh37.p13 chr6: 42,511,039-43,009,338 , RPL7L1, 20 more genes
    nsv5117647mobile element insertion1nstd203human GRCh38 chr6: 42,935,946-42,935,953 , GRCh37.p13 chr6: 42,903,684-42,903,691 CNPY3, CNPY3-GNMT
    nsv5116181mobile element insertion1nstd203human GRCh38 chr6: 42,935,941-42,935,953 , GRCh37.p13 chr6: 42,903,679-42,903,691 CNPY3-GNMT, CNPY3
    nsv5108968mobile element insertion1nstd203human GRCh38 chr6: 42,935,945-42,935,953 , GRCh37.p13 chr6: 42,903,683-42,903,691 CNPY3-GNMT, CNPY3
    nsv5103372mobile element insertion1nstd203human GRCh38 chr6: 42,935,948-42,935,953 , GRCh37.p13 chr6: 42,903,686-42,903,691 CNPY3-GNMT, CNPY3
    nsv5102179mobile element insertion1nstd203human GRCh38 chr6: 42,935,032-42,935,047 , GRCh37.p13 chr6: 42,902,770-42,902,785 CNPY3, CNPY3-GNMT
    nsv5101750mobile element insertion1nstd203human GRCh38 chr6: 42,935,944-42,935,953 , GRCh37.p13 chr6: 42,903,682-42,903,691 CNPY3-GNMT, CNPY3
    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
    nsv4750468insertion1nstd199human GRCh37 chr6: 42,903,831-42,903,831 , GRCh38.p12 chr6: 42,936,093-42,936,093 CNPY3, CNPY3-GNMT
    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
    nsv4682355copy number variation1nstd102humanUncertain significance GRCh37 chr6: 42,890,765-42,952,442 , GRCh38.p12 chr6: 42,923,027-42,984,704 MEA1, CNPY3-GNMT, 6 more genes
    nsv4652620copy number variation1nstd186human GRCh37 chr6: 42,903,834-42,903,912 , GRCh38.p12 chr6: 42,936,096-42,936,174 CNPY3, CNPY3-GNMT
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