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Items: 1 to 20 of 651

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5972619inversion1nstd209human GRCh38 chr6: 139,184,023-139,187,671 , GRCh37.p13 chr6: 139,505,160-139,508,808 TXLNB
    nsv5906712copy number variation1nstd209human GRCh38 chr6: 139,307,965-139,308,014 , GRCh37.p13 chr6: 139,629,102-139,629,151 TXLNB
    nsv5903720copy number variation1nstd209human GRCh38 chr6: 139,188,724-139,188,836 , GRCh37.p13 chr6: 139,509,861-139,509,973 TXLNB
    nsv5898323copy number variation1nstd209human GRCh38 chr6: 139,321,840-139,323,548 , GRCh37.p13 chr6: 139,642,977-139,644,685 TXLNB
    nsv5895687copy number variation1nstd209human GRCh38 chr6: 139,281,461-139,286,010 , GRCh37.p13 chr6: 139,602,598-139,607,147 LOC102723690, TXLNB
    nsv5893658copy number variation1nstd209human GRCh38 chr6: 139,162,641-139,165,509 , GRCh37.p13 chr6: 139,483,778-139,486,646 HECA, TXLNB
    nsv5889737copy number variation1nstd209human GRCh38 chr6: 139,281,530-139,281,846 , GRCh37.p13 chr6: 139,602,667-139,602,983 LOC102723690, TXLNB
    nsv5844395copy number variation1nstd209human GRCh38 chr6: 139,183,969-139,192,883 , GRCh37.p13 chr6: 139,505,106-139,514,020 TXLNB
    nsv5844302copy number variation1nstd209human GRCh38 chr6: 139,162,342-139,165,593 , GRCh37.p13 chr6: 139,483,479-139,486,730 HECA, TXLNB
    nsv5844048copy number variation1nstd209human GRCh38 chr6: 139,282,270-139,286,035 , GRCh37.p13 chr6: 139,603,407-139,607,172 LOC102723690, TXLNB
    nsv5844047copy number variation1nstd209human GRCh38 chr6: 139,212,839-139,223,199 , GRCh37.p13 chr6: 139,533,976-139,544,336 TXLNB
    nsv5718198mobile element insertion1nstd211human GRCh38 chr6: 139,242,202-139,242,202 , GRCh37.p13 chr6: 139,563,339-139,563,339 TXLNB
    nsv5688512mobile element insertion2nstd211human GRCh38 chr6: 139,183,874-139,183,874 , GRCh37.p13 chr6: 139,505,011-139,505,011 TXLNB
    nsv5688033mobile element insertion1nstd211human GRCh38 chr6: 139,193,260-139,193,260 , GRCh37.p13 chr6: 139,514,397-139,514,397 TXLNB
    nsv5684515mobile element insertion2nstd211human GRCh38 chr6: 139,318,500-139,318,500 , GRCh37.p13 chr6: 139,639,637-139,639,637 TXLNB
    nsv5683694mobile element insertion1nstd211human GRCh38 chr6: 139,296,399-139,296,399 , GRCh37.p13 chr6: 139,617,536-139,617,536 TXLNB
    nsv5682032mobile element insertion1nstd211human GRCh38 chr6: 139,247,556-139,247,556 , GRCh37.p13 chr6: 139,568,693-139,568,693 TXLNB
    nsv5641487insertion1nstd207human GRCh38 chr6: 139,183,860-139,183,860 , GRCh37.p13 chr6: 139,504,997-139,504,997 TXLNB
    nsv5641064insertion1nstd207human GRCh38 chr6: 139,318,487-139,318,487 , GRCh37.p13 chr6: 139,639,624-139,639,624 TXLNB
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