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Items: 1 to 20 of 189

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5954666insertion1nstd209human GRCh38 chr2: 69,859,742-69,859,742 , GRCh37.p13 chr2: 70,086,874-70,086,874 GMCL1
    nsv5877622copy number variation1nstd209human GRCh38 chr2: 69,847,687-69,847,796 , GRCh37.p13 chr2: 70,074,819-70,074,928 GMCL1
    nsv5871128copy number variation1nstd209human GRCh38 chr2: 69,851,172-69,851,315 , GRCh37.p13 chr2: 70,078,304-70,078,447 GMCL1
    nsv5716041mobile element insertion2nstd211human GRCh38 chr2: 69,833,265-69,833,265 , GRCh37.p13 chr2: 70,060,397-70,060,397 GMCL1
    nsv5558049mobile element insertion1nstd206human GRCh38 chr2: 69,833,265-69,833,316 , GRCh37.p13 chr2: 70,060,397-70,060,448 GMCL1
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5437622copy number variation1nstd206human GRCh38 chr2: 69,847,691-69,847,797 , GRCh37.p13 chr2: 70,074,823-70,074,929 GMCL1
    nsv5435629copy number variation1nstd206human GRCh38 chr2: 69,853,375-69,854,687 , GRCh37.p13 chr2: 70,080,507-70,081,819 GMCL1
    nsv5360763translocation1nstd200human GRCh38 chr2: 69,878,195-69,878,195 , GRCh38 chr2: 69,878,133-69,878,133 , GRCh37.p13 chr2: 70,105,265-70,105,265 , GRCh37.p13 chr2: 70,105,327-70,105,327 GMCL1
    nsv5360762translocation1nstd200human GRCh38 chr2: 69,847,691-69,847,691 , GRCh38 chr2: 69,847,797-69,847,797 , GRCh37.p13 chr2: 70,074,823-70,074,823 , GRCh37.p13 chr2: 70,074,929-70,074,929 GMCL1
    nsv5340281translocation1nstd200human GRCh37 chr2: 70,074,929-70,074,929 , GRCh37 chr2: 70,074,823-70,074,823 , GRCh38.p12 chr2: 69,847,691-69,847,691 , GRCh38.p12 chr2: 69,847,797-69,847,797 GMCL1
    nsv5174659mobile element insertion1nstd203human GRCh38 chr2: 69,833,248-69,833,265 , GRCh37.p13 chr2: 70,060,380-70,060,397 GMCL1
    nsv5078906mobile element insertion1nstd203human GRCh38 chr2: 69,841,160-69,841,176 , GRCh37.p13 chr2: 70,068,292-70,068,308 GMCL1
    nsv5062515mobile element insertion1nstd203human GRCh38 chr2: 69,832,818-69,832,833 , GRCh37.p13 chr2: 70,059,950-70,059,965 GMCL1
    nsv4908790copy number variation1nstd200human GRCh38 chr2: 69,781,324-69,828,498 , GRCh37.p13 chr2: 70,008,456-70,055,630 ANXA4, GMCL1, 1 more genes
    nsv4757601insertion1nstd199human GRCh37 chr2: 70,060,397-70,060,397 , GRCh38.p12 chr2: 69,833,265-69,833,265 GMCL1
    nsv4728508copy number variation1nstd102humanUncertain significance GRCh37 chr2: 69,506,803-70,159,981 , GRCh38.p12 chr2: 69,279,671-69,932,849 SNORA36C, GFPT1, 12 more genes
    nsv4584380copy number variation2nstd183human GRCh37 chr2: 70,082,405-70,088,696 , GRCh38.p12 chr2: 69,855,273-69,861,564 GMCL1
    nsv4584090copy number variation1nstd183human GRCh37 chr2: 70,081,783-70,082,348 , GRCh38.p12 chr2: 69,854,651-69,855,216 GMCL1
    nsv4584089copy number variation1nstd183human GRCh37 chr2: 70,061,019-70,064,716 , GRCh38.p12 chr2: 69,833,887-69,837,584 GMCL1
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