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Items: 1 to 20 of 239

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5692874mobile element insertion1nstd211human GRCh38 chr6: 139,770,559-139,770,559 , GRCh37.p13 chr6: 140,091,696-140,091,696 FILNC1
    nsv5686771mobile element insertion2nstd211human GRCh38 chr6: 139,781,732-139,781,732 , GRCh37.p13 chr6: 140,102,869-140,102,869 FILNC1
    nsv5456170copy number variation1nstd206human GRCh38 chr6: 139,844,895-139,844,957 , GRCh37.p13 chr6: 140,166,032-140,166,094 FILNC1
    nsv5394221mobile element insertion1nstd206human GRCh38 chr6: 139,781,732-139,781,783 , GRCh37.p13 chr6: 140,102,869-140,102,920 FILNC1
    nsv5363418translocation1nstd200human GRCh38 chr6: 139,821,071-139,821,071 , GRCh38 chr6: 139,821,985-139,821,985 , GRCh37.p13 chr6: 140,143,122-140,143,122 , GRCh37.p13 chr6: 140,142,208-140,142,208 FILNC1
    nsv5236971copy number variation1nstd204human GRCh38.p13 chr6: 139,790,001-139,792,400 , GRCh37.p13 chr6: 140,111,138-140,113,537 FILNC1
    nsv5232530copy number variation1nstd204human GRCh38.p13 chr6: 139,860,526-139,862,725 , GRCh37.p13 chr6: 140,181,663-140,183,862 FILNC1
    nsv5039909inversion1nstd200human GRCh38 chr6: 137,955,606-139,947,661 , GRCh37.p13 chr6: 138,276,743-140,268,798 , CCDC28A-AS1, 30 more genes
    nsv4942970copy number variation1nstd200human GRCh38 chr6: 139,844,895-139,844,957 , GRCh37.p13 chr6: 140,166,032-140,166,094 FILNC1
    nsv4942969copy number variation1nstd200human GRCh38 chr6: 139,775,534-139,851,572 , GRCh37.p13 chr6: 140,096,671-140,172,709 FILNC1
    nsv4942968copy number variation1nstd200human GRCh38 chr6: 139,770,190-139,771,519 , GRCh37.p13 chr6: 140,091,327-140,092,656 FILNC1
    nsv4942967copy number variation1nstd200human GRCh38 chr6: 139,765,294-139,981,536 , GRCh37.p13 chr6: 140,086,431-140,302,673 LINC02941, FILNC1, 1 more genes
    nsv4810618copy number variation1nstd200human GRCh37 chr6: 140,166,032-140,166,094 , GRCh38.p12 chr6: 139,844,895-139,844,957 FILNC1
    nsv4810617copy number variation1nstd200human GRCh37 chr6: 140,096,671-140,172,709 , GRCh38.p12 chr6: 139,775,534-139,851,572 FILNC1
    nsv4810616copy number variation1nstd200human GRCh37 chr6: 140,091,327-140,092,656 , GRCh38.p12 chr6: 139,770,190-139,771,519 FILNC1
    nsv4685709copy number variation1nstd102humannot provided GRCh37 chr6: 135,936,688-140,660,269 , GRCh38.p12 chr6: 135,615,550-140,339,132 MAP7, RN7SKP299, 74 more genes
    nsv4610610copy number variation1nstd183human GRCh37 chr6: 140,127,307-140,144,919 , GRCh38.p12 chr6: 139,806,170-139,823,782 FILNC1
    nsv4609603copy number variation1nstd183human GRCh37 chr6: 140,116,578-140,129,526 , GRCh38.p12 chr6: 139,795,441-139,808,389 FILNC1
    nsv4498060mobile element insertion1nstd166human GRCh37.p13 chr6: 140,102,853-140,102,853 , GRCh38.p12 chr6: 139,781,716-139,781,716 FILNC1
    nsv4480507mobile element insertion1nstd166human GRCh37.p13 chr6: 140,102,739-140,102,739 , GRCh38.p12 chr6: 139,781,602-139,781,602 FILNC1
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