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Items: 1 to 20 of 151

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097826copy number variation1nstd102humanPathogenic GRCh37 chr6: 41,126,341-43,752,536 , GRCh38.p12 chr6: 41,158,603-43,784,799 USP49, PRICKLE4, 96 more genes
    nsv7097825copy number variation1nstd102humanUncertain significance GRCh37 chr6: 41,126,341-43,737,486 , GRCh38.p12 chr6: 41,158,603-43,769,749 DNPH1, LOC107986596, 96 more genes
    nsv7097331copy number variation1nstd102humanUncertain significance GRCh37 chr6: 42,162,409-44,154,249 , GRCh38.p12 chr6: 42,194,671-44,186,512 MRPS10, CUL9, 70 more genes
    nsv7043293inversion1nstd229human GRCh38 chr6: 39,854,165-43,261,822 , GRCh37.p13 chr6: 39,821,941-43,229,560 RPL23P6, RPL32P15, 95 more genes
    nsv6795859copy number variation1nstd229human GRCh38 chr6: 42,181,001-42,186,900 , GRCh37.p13 chr6: 42,148,739-42,154,638 GUCA1B
    nsv6789272copy number variation1nstd229human GRCh38 chr6: 41,897,601-42,523,500 , GRCh37.p13 chr6: 41,865,339-42,491,238 LOC105375061, RPL36AP5, 13 more genes
    nsv6636814copy number variation1nstd102humanUncertain significance GRCh37 chr6: 42,043,510-42,274,148 , GRCh38.p12 chr6: 42,075,772-42,306,410 TRERF1, LOC105375061, 6 more genes
    nsv6631499copy number variation1nstd224human GRCh37 chr6: 42,074,371-42,153,535 , GRCh38.p12 chr6: 42,106,633-42,185,797 GUCA1A, C6orf132, 2 more genes
    nsv6570897inversion1nstd223human GRCh38 chr6: 42,195,059-42,196,077 , GRCh37.p13 chr6: 42,162,797-42,163,815 GUCA1B
    nsv6568986inversion1nstd223human GRCh38 chr6: 42,195,180-42,196,452 , GRCh37.p13 chr6: 42,162,918-42,164,190 GUCA1B
    nsv6566770inversion1nstd223human GRCh38 chr6: 42,194,666-44,186,502 , GRCh37.p13 chr6: 42,162,404-44,154,239 RPL36AP5, MIR6780B, 70 more genes
    nsv6565260inversion1nstd223human GRCh38 chr6: 42,186,474-42,187,162 , GRCh37.p13 chr6: 42,154,212-42,154,900 GUCA1B
    nsv6562590inversion1nstd223human GRCh38 chr6: 42,195,350-42,196,126 , GRCh37.p13 chr6: 42,163,088-42,163,864 GUCA1B
    nsv6280350insertion1nstd214human GRCh38 chr6: 42,188,893-42,188,893 , GRCh37.p13 chr6: 42,156,631-42,156,631 GUCA1B
    nsv6135921copy number variation1nstd213human GRCh37 chr6: 34,700,000-52,650,001 , GRCh38.p12 chr6: 34,732,223-52,785,203 ACTG1P9, CRISP1, 361 more genes
    nsv5957481insertion1nstd209human GRCh38 chr6: 42,188,893-42,188,893 , GRCh37.p13 chr6: 42,156,631-42,156,631 GUCA1B
    nsv5952630insertion1nstd209human GRCh38 chr6: 42,192,380-42,192,380 , GRCh37.p13 chr6: 42,160,118-42,160,118 GUCA1B
    nsv5564439copy number variation1nstd102humanUncertain significance GRCh37 chr6: 42,152,553-42,153,535 , GRCh38.p12 chr6: 42,184,815-42,185,797 GUCA1B
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5550060insertion1nstd206human GRCh38 chr6: 42,188,896-42,188,938 , GRCh37.p13 chr6: 42,156,634-42,156,676 GUCA1B
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