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Items: 1 to 20 of 166

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6129775insertion1nstd186human GRCh37 chr22: 40,403,331-40,403,331 , GRCh38.p12 chr22: 40,007,327-40,007,327 FAM83F
    nsv5961865copy number variation1nstd209human GRCh38 chr22: 40,012,727-40,013,039 , GRCh37.p13 chr22: 40,408,731-40,409,043 FAM83F
    nsv5718200mobile element insertion1nstd211human GRCh38 chr22: 39,996,530-39,996,530 , GRCh37.p13 chr22: 40,392,534-40,392,534 FAM83F
    nsv5667099insertion1nstd207human GRCh38 chr22: 40,007,327-40,007,327 , GRCh37.p13 chr22: 40,403,331-40,403,331 FAM83F
    nsv5558188mobile element insertion1nstd206human GRCh38 chr22: 39,996,530-39,996,581 , GRCh37.p13 chr22: 40,392,534-40,392,585 FAM83F
    nsv5549658copy number variation1nstd206human GRCh38 chr22: 40,011,207-40,020,424 , GRCh37.p13 chr22: 40,407,211-40,416,428 FAM83F
    nsv5544974copy number variation1nstd206human GRCh38 chr22: 40,027,720-40,035,732 , GRCh37.p13 chr22: 40,423,724-40,431,736 FAM83F
    nsv5539354copy number variation1nstd206human GRCh38 chr22: 39,997,541-40,001,275 , GRCh37.p13 chr22: 40,393,545-40,397,279 FAM83F
    nsv5539154insertion1nstd206human GRCh38 chr22: 40,007,327-40,007,327 , GRCh37.p13 chr22: 40,403,331-40,403,331 FAM83F
    nsv5375705translocation1nstd200human GRCh38 chr22: 40,038,581-40,038,581 , GRCh38 chr22: 40,039,191-40,039,191 , GRCh37.p13 chr22: 40,434,585-40,434,585 , GRCh37.p13 chr22: 40,435,195-40,435,195 FAM83F
    nsv5375704translocation1nstd200human GRCh38 chr22: 40,039,249-40,039,249 , GRCh38 chr22: 40,037,356-40,037,356 , GRCh37.p13 chr22: 40,433,360-40,433,360 , GRCh37.p13 chr22: 40,435,253-40,435,253 FAM83F
    nsv5360589translocation1nstd200human GRCh38 chr22: 40,001,275-40,001,275 , GRCh38 chr22: 39,997,541-39,997,541 , GRCh37.p13 chr22: 40,397,279-40,397,279 , GRCh37.p13 chr22: 40,393,545-40,393,545 FAM83F
    nsv5341502translocation1nstd200human GRCh37 chr22: 40,434,585-40,434,585 , GRCh37 chr22: 40,435,195-40,435,195 , GRCh38.p12 chr22: 40,038,581-40,038,581 , GRCh38.p12 chr22: 40,039,191-40,039,191 FAM83F
    nsv5340739translocation1nstd200human GRCh37 chr22: 40,435,253-40,435,253 , GRCh37 chr22: 40,433,360-40,433,360 , GRCh38.p12 chr22: 40,039,249-40,039,249 , GRCh38.p12 chr22: 40,037,356-40,037,356 FAM83F
    nsv5323120copy number variation1nstd204human GRCh38.p13 chr22: 39,997,518-40,001,296 , GRCh37.p13 chr22: 40,393,522-40,397,300 FAM83F
    nsv5291338copy number variation1nstd204human GRCh38.p13 chr22: 39,997,496-40,001,424 , GRCh37.p13 chr22: 40,393,500-40,397,428 FAM83F
    nsv5283166copy number variation1nstd204human GRCh38.p13 chr22: 39,997,501-40,001,300 , GRCh37.p13 chr22: 40,393,505-40,397,304 FAM83F
    nsv5178061mobile element insertion1nstd203human GRCh38 chr22: 40,007,564-40,007,583 , GRCh37.p13 chr22: 40,403,568-40,403,587 FAM83F
    nsv5176231mobile element insertion1nstd203human GRCh38 chr22: 40,007,247-40,007,247 , GRCh37.p13 chr22: 40,403,251-40,403,251 FAM83F
    nsv5172583mobile element insertion1nstd203human GRCh38 chr22: 40,007,372-40,007,372 , GRCh37.p13 chr22: 40,403,376-40,403,376 FAM83F
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