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Items: 1 to 20 of 348

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094335copy number variation1nstd102humanPathogenic GRCh37 chr14: 50,750,569-50,750,771 , GRCh38.p12 chr14: 50,283,851-50,284,053 L2HGDH
    nsv7094333copy number variation1nstd102humanUncertain significance GRCh37 chr14: 50,641,152-50,778,868 , GRCh38.p12 chr14: 50,174,434-50,312,150 SOS2, L2HGDH, 2 more genes
    nsv7094254copy number variation1nstd102humanPathogenic GRCh37 chr14: 50,760,813-50,768,906 , GRCh38.p12 chr14: 50,294,095-50,302,188 MIR4504, L2HGDH
    nsv7076302inversion1nstd229human GRCh38 chr14: 46,512,743-51,785,975 , GRCh37.p13 chr14: 46,981,946-52,252,693 LOC100420098, MAP4K5, 82 more genes
    nsv7075600inversion1nstd229human GRCh38 chr14: 50,269,524-50,269,620 , GRCh37.p13 chr14: 50,736,242-50,736,338 L2HGDH
    nsv7063700inversion1nstd229human GRCh38 chr14: 48,591,726-55,698,685 , GRCh37.p13 chr14: 49,060,929-56,165,403 ZFP64P1, LINC02331, 132 more genes
    nsv7059291inversion1nstd229human GRCh38 chr14: 49,838,942-56,572,993 , GRCh37.p13 chr14: 50,305,660-57,039,711 LOC105370500, LINC01599, 124 more genes
    nsv6953489copy number variation1nstd229human GRCh38 chr14: 50,257,204-50,265,795 , GRCh37.p13 chr14: 50,723,922-50,732,513 L2HGDH
    nsv6951991copy number variation1nstd229human GRCh38 chr14: 50,288,625-50,393,821 , GRCh37.p13 chr14: 50,755,343-50,860,539 DMAC2L, MIR4504, 2 more genes
    nsv6950422copy number variation1nstd229human GRCh38 chr14: 50,251,301-50,260,300 , GRCh37.p13 chr14: 50,718,019-50,727,018 L2HGDH
    nsv6949584copy number variation1nstd229human GRCh38 chr14: 50,251,201-50,260,200 , GRCh37.p13 chr14: 50,717,919-50,726,918 L2HGDH
    nsv6947339copy number variation1nstd229human GRCh38 chr14: 50,283,504-50,291,845 , GRCh37.p13 chr14: 50,750,222-50,758,563 L2HGDH
    nsv6947197copy number variation1nstd229human GRCh38 chr14: 50,249,501-50,260,300 , GRCh37.p13 chr14: 50,716,219-50,727,018 L2HGDH
    nsv6945576copy number variation1nstd229human GRCh38 chr14: 50,268,448-50,289,703 , GRCh37.p13 chr14: 50,735,166-50,756,421 L2HGDH
    nsv6942228copy number variation1nstd229human GRCh38 chr14: 50,290,495-50,365,602 , GRCh37.p13 chr14: 50,757,213-50,832,320 MIR4504, DMAC2L, 2 more genes
    nsv6942097copy number variation1nstd229human GRCh38 chr14: 50,251,101-50,262,100 , GRCh37.p13 chr14: 50,717,819-50,728,818 L2HGDH
    nsv6941650copy number variation1nstd229human GRCh38 chr14: 50,304,730-50,308,723 , GRCh37.p13 chr14: 50,771,448-50,775,441 L2HGDH
    nsv6941214copy number variation1nstd229human GRCh38 chr14: 50,292,090-50,292,606 , GRCh37.p13 chr14: 50,758,808-50,759,324 L2HGDH
    nsv6940638copy number variation1nstd229human GRCh38 chr14: 50,247,980-50,250,082 , GRCh37.p13 chr14: 50,714,698-50,716,800 L2HGDH
    nsv6938683copy number variation1nstd229human GRCh38 chr14: 50,250,592-50,306,669 , GRCh37.p13 chr14: 50,717,310-50,773,387 MIR4504, L2HGDH
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