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Items: 1 to 20 of 516

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5959983insertion1nstd209human GRCh38 chr3: 50,025,592-50,025,592 , GRCh37.p13 chr3: 50,063,025-50,063,025 RBM6
    nsv5904094copy number variation1nstd209human GRCh38 chr3: 49,948,710-49,955,680 , GRCh37.p13 chr3: 49,986,143-49,993,113 RBM6
    nsv5898113copy number variation1nstd209human GRCh38 chr3: 50,043,834-50,044,129 , GRCh37.p13 chr3: 50,081,267-50,081,562 RBM6
    nsv5897437copy number variation1nstd209human GRCh38 chr3: 49,938,767-49,939,538 , GRCh37.p13 chr3: 49,976,200-49,976,971 RBM6
    nsv5891025copy number variation1nstd209human GRCh38 chr3: 49,693,626-52,462,904 , GRCh37.p13 chr3: 49,731,059-52,496,920 , SEMA3G, 106 more genes
    nsv5890155copy number variation1nstd209human GRCh38 chr3: 49,955,118-49,956,675 , GRCh37.p13 chr3: 49,992,551-49,994,108 RBM6
    nsv5836361copy number variation1nstd209human GRCh38 chr3: 50,012,512-50,018,442 , GRCh37.p13 chr3: 50,049,945-50,055,875 RBM6
    nsv5836360copy number variation1nstd209human GRCh38 chr3: 49,948,494-49,954,938 , GRCh37.p13 chr3: 49,985,927-49,992,371 RBM6
    nsv5690475mobile element insertion1nstd211human GRCh38 chr3: 49,996,483-49,996,483 , GRCh37.p13 chr3: 50,033,916-50,033,916 RBM6
    nsv5689167mobile element insertion2nstd211human GRCh38 chr3: 50,025,606-50,025,606 , GRCh37.p13 chr3: 50,063,039-50,063,039 RBM6
    nsv5673729copy number variation1nstd102humanPathogenic GRCh37 chr3: 48,507,870-50,340,407 , GRCh38.p12 chr3: 48,466,471-50,302,976 SEMA3B-AS1, GNAT1, 87 more genes
    nsv5617010insertion1nstd207human GRCh38 chr3: 50,025,592-50,025,592 , GRCh37.p13 chr3: 50,063,025-50,063,025 RBM6
    nsv5572014copy number variation1nstd207human GRCh38 chr3: 49,938,711-49,939,483 , GRCh37.p13 chr3: 49,976,144-49,976,916 RBM6
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5546282insertion1nstd206human GRCh38 chr3: 50,025,592-50,025,592 , GRCh37.p13 chr3: 50,063,025-50,063,025 RBM6
    nsv5453349copy number variation1nstd206human GRCh38 chr3: 49,939,069-49,939,483 , GRCh37.p13 chr3: 49,976,502-49,976,916 RBM6
    nsv5452742copy number variation1nstd206human GRCh38 chr3: 49,938,814-49,939,223 , GRCh37.p13 chr3: 49,976,247-49,976,656 RBM6
    nsv5452397copy number variation1nstd206human GRCh38 chr3: 49,958,320-49,962,169 , GRCh37.p13 chr3: 49,995,753-49,999,602 RBM6
    nsv5451568copy number variation1nstd206human GRCh38 chr3: 49,955,201-49,955,432 , GRCh37.p13 chr3: 49,992,634-49,992,865 RBM6
    nsv5445642copy number variation1nstd206human GRCh38 chr3: 49,944,567-49,946,604 , GRCh37.p13 chr3: 49,982,000-49,984,037 RBM6
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