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Items: 1 to 20 of 244

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5835011copy number variation1nstd209human GRCh38 chr3: 155,928,607-155,931,898 , GRCh37.p13 chr3: 155,646,396-155,649,687 GMPS
    nsv5835010copy number variation1nstd209human GRCh38 chr3: 155,879,766-155,886,429 , GRCh37.p13 chr3: 155,597,555-155,604,218 GMPS
    nsv5729732mobile element insertion1nstd211human GRCh38 chr3: 155,938,948-155,938,948 , GRCh37.p13 chr3: 155,656,737-155,656,737 GMPS
    nsv5691307mobile element insertion1nstd211human GRCh38 chr3: 155,892,198-155,892,198 , GRCh37.p13 chr3: 155,609,987-155,609,987 GMPS
    nsv5681665mobile element insertion1nstd211human GRCh38 chr3: 155,920,804-155,920,804 , GRCh37.p13 chr3: 155,638,593-155,638,593 GMPS
    nsv5676024mobile element insertion1nstd211human GRCh38 chr3: 155,896,752-155,896,752 , GRCh37.p13 chr3: 155,614,541-155,614,541 GMPS
    nsv5561796sequence alteration1nstd206human GRCh38 chr3: 155,894,150-155,894,754 , GRCh37.p13 chr3: 155,611,939-155,612,543 GMPS
    nsv5539161insertion1nstd206human GRCh38 chr3: 155,894,151-155,894,151 , GRCh37.p13 chr3: 155,611,940-155,611,940 GMPS
    nsv5452284copy number variation1nstd206human GRCh38 chr3: 155,877,738-155,897,816 , GRCh37.p13 chr3: 155,595,527-155,615,605 GMPS
    nsv5447381copy number variation1nstd206human GRCh38 chr3: 155,870,487-155,870,543 , GRCh37.p13 chr3: 155,588,276-155,588,332 GMPS
    nsv5445714copy number variation1nstd206human GRCh38 chr3: 154,528,533-156,057,304 , GRCh37.p13 chr3: 154,246,322-155,775,093 LINC01487, MME, 21 more genes
    nsv5434568copy number variation1nstd206human GRCh38 chr3: 155,900,067-155,900,187 , GRCh37.p13 chr3: 155,617,856-155,617,976 GMPS
    nsv5413895mobile element insertion1nstd206human GRCh38 chr3: 155,892,198-155,892,249 , GRCh37.p13 chr3: 155,609,987-155,610,038 GMPS
    nsv5401266mobile element insertion1nstd206human GRCh38 chr3: 155,920,804-155,920,855 , GRCh37.p13 chr3: 155,638,593-155,638,644 GMPS
    nsv5381765copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,173,683-162,494,699 , GRCh38.p12 chr3: 138,454,841-162,776,911 MBNL1-AS1, LOC107986138, 339 more genes
    nsv5343065translocation1nstd200human GRCh37 chr3: 155,612,543-155,612,543 , GRCh37 chr3: 155,611,940-155,611,940 , GRCh38.p12 chr3: 155,894,754-155,894,754 , GRCh38.p12 chr3: 155,894,151-155,894,151 GMPS
    nsv5326759translocation1nstd204human GRCh38.p13 chr3: 155,894,151-155,894,151 , GRCh38.p13 chr3: 155,894,754-155,894,754 , GRCh37.p13 chr3: 155,611,940-155,611,940 , GRCh37.p13 chr3: 155,612,543-155,612,543 GMPS
    nsv5320012copy number variation1nstd204human GRCh38.p13 chr3: 155,909,705-155,909,978 , GRCh37.p13 chr3: 155,627,494-155,627,767 GMPS
    nsv5196650mobile element insertion1nstd203human GRCh38 chr3: 155,869,844-155,869,861 , GRCh37.p13 chr3: 155,587,633-155,587,650 GMPS
    nsv5097730mobile element insertion1nstd203human GRCh38 chr3: 155,868,021-155,868,021 , GRCh37.p13 chr3: 155,585,810-155,585,810 GMPS
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