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Items: 1 to 20 of 202

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7050559inversion1nstd229human GRCh38 chr6: 137,097,512-142,245,470 , GRCh37.p13 chr6: 137,418,649-142,566,607 LINC03004, LOC107986651, 64 more genes
    nsv6816096copy number variation1nstd229human GRCh38 chr6: 139,162,643-139,165,513 , GRCh37.p13 chr6: 139,483,780-139,486,650 HECA, TXLNB
    nsv6811912copy number variation1nstd229human GRCh38 chr6: 137,801,388-140,356,633 , GRCh37.p13 chr6: 138,122,525-140,677,770 TXLNB, LOC100129844, 38 more genes
    nsv6809593copy number variation1nstd229human GRCh38 chr6: 139,140,720-139,141,077 , GRCh37.p13 chr6: 139,461,857-139,462,214 HECA
    nsv6807463copy number variation1nstd229human GRCh38 chr6: 139,139,030-139,143,187 , GRCh37.p13 chr6: 139,460,167-139,464,324 HECA
    nsv6807031copy number variation1nstd229human GRCh38 chr6: 139,143,539-139,143,900 , GRCh37.p13 chr6: 139,464,676-139,465,037 HECA
    nsv6806866copy number variation1nstd229human GRCh38 chr6: 139,140,442-139,141,464 , GRCh37.p13 chr6: 139,461,579-139,462,601 HECA
    nsv6806243copy number variation1nstd229human GRCh38 chr6: 139,179,988-139,193,246 , GRCh37.p13 chr6: 139,501,125-139,514,383 HECA, TXLNB
    nsv6803308copy number variation1nstd229human GRCh38 chr6: 139,139,101-139,143,200 , GRCh37.p13 chr6: 139,460,238-139,464,337 HECA
    nsv6607899copy number variation1nstd223human GRCh38 chr6: 139,140,442-139,141,464 , GRCh37.p13 chr6: 139,461,579-139,462,601 HECA
    nsv6314818copy number variation1nstd102humanPathogenic GRCh38 chr6: 134,838,331-142,160,056 , GRCh37.p13 chr6: 135,159,469-142,481,193 PBOV1, IFNGR1, 100 more genes
    nsv6313861copy number variation1nstd102humanUncertain significance GRCh37 chr6: 139,093,282-140,660,265 , GRCh38.p12 chr6: 138,772,145-140,339,128 LINC01625, ECT2L, 23 more genes
    nsv6257257mobile element insertion1nstd215human GRCh38 chr6: 139,174,837-139,174,837 , GRCh37.p13 chr6: 139,495,974-139,495,974 HECA, TXLNB
    nsv6112726copy number variation1nstd102humanPathogenic GRCh37 chr6: 133,810,210-140,046,615 , GRCh38.p12 chr6: 133,489,072-139,725,478 SIMALR, MTFR2, 99 more genes
    nsv5893658copy number variation1nstd209human GRCh38 chr6: 139,162,641-139,165,509 , GRCh37.p13 chr6: 139,483,778-139,486,646 HECA, TXLNB
    nsv5844302copy number variation1nstd209human GRCh38 chr6: 139,162,342-139,165,593 , GRCh37.p13 chr6: 139,483,479-139,486,730 HECA, TXLNB
    nsv5560252sequence alteration1nstd206human GRCh38 chr6: 139,156,973-139,161,033 , GRCh37.p13 chr6: 139,478,110-139,482,170 HECA, TXLNB
    nsv5551978insertion1nstd206human GRCh38 chr6: 139,161,032-139,161,032 , GRCh37.p13 chr6: 139,482,169-139,482,169 TXLNB, HECA
    nsv5460181copy number variation1nstd206human GRCh38 chr6: 139,143,590-139,158,205 , GRCh37.p13 chr6: 139,464,727-139,479,342 HECA, TXLNB
    nsv5039909inversion1nstd200human GRCh38 chr6: 137,955,606-139,947,661 , GRCh37.p13 chr6: 138,276,743-140,268,798 , CCDC28A-AS1, 30 more genes
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