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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
    nsv5947429copy number variation1nstd209human GRCh38 chr19: 45,811,656-45,813,564 , GRCh37.p13 chr19: 46,314,914-46,316,822 RSPH6A, SYMPK
    nsv5940606copy number variation1nstd209human GRCh38 chr19: 45,857,519-45,858,677 , GRCh37.p13 chr19: 46,360,777-46,361,935 SYMPK
    nsv5868422copy number variation1nstd209human GRCh38 chr19: 45,811,658-45,813,604 , GRCh37.p13 chr19: 46,314,916-46,316,862 RSPH6A, SYMPK
    nsv5727000mobile element insertion2nstd211human GRCh38 chr19: 45,841,689-45,841,689 , GRCh37.p13 chr19: 46,344,947-46,344,947 SYMPK
    nsv5603885copy number variation1nstd207human GRCh38 chr19: 45,811,656-45,813,564 , GRCh37.p13 chr19: 46,314,914-46,316,822 RSPH6A, SYMPK
    nsv5555882sequence alteration1nstd206human GRCh38 chr19: 45,580,124-46,272,839 , GRCh37.p13 chr19: 46,083,382-46,776,096 , SYMPK, 39 more genes
    nsv5554586mobile element insertion1nstd206human GRCh38 chr19: 45,841,689-45,841,740 , GRCh37.p13 chr19: 46,344,947-46,344,998 SYMPK
    nsv5517769copy number variation1nstd206human GRCh38 chr19: 45,844,370-45,846,052 , GRCh37.p13 chr19: 46,347,628-46,349,310 SYMPK
    nsv5516766copy number variation1nstd206human GRCh38 chr19: 45,811,949-45,813,644 , GRCh37.p13 chr19: 46,315,207-46,316,902 SYMPK, RSPH6A
    nsv5359847translocation1nstd200human GRCh38 chr19: 45,861,135-45,861,135 , GRCh38 chr19: 45,861,052-45,861,052 , GRCh37.p13 chr19: 46,364,310-46,364,310 , GRCh37.p13 chr19: 46,364,393-46,364,393 SYMPK
    nsv5359846translocation1nstd200human GRCh38 chr19: 45,828,073-45,828,073 , GRCh38 chr19: 45,828,361-45,828,361 , GRCh37.p13 chr19: 46,331,331-46,331,331 , GRCh37.p13 chr19: 46,331,619-46,331,619 SYMPK
    nsv5327341copy number variation1nstd204human GRCh38.p13 chr19: 45,584,936-45,884,300 , GRCh37.p13 chr19: 46,088,194-46,387,558 DMWD, GPR4, 19 more genes
    nsv5324517copy number variation1nstd204human GRCh37.p13 chr19: 46,314,925-46,316,797 , GRCh38.p13 chr19: 45,811,667-45,813,539 SYMPK, RSPH6A
    nsv5300097copy number variation1nstd204human GRCh38.p13 chr19: 45,810,833-45,825,471 , GRCh37.p13 chr19: 46,314,091-46,328,729 RSPH6A, SYMPK
    nsv5289939copy number variation1nstd204human GRCh38.p13 chr19: 45,838,215-45,844,291 , GRCh37.p13 chr19: 46,341,473-46,347,549 SYMPK
    nsv5286410copy number variation1nstd204human GRCh38.p13 chr19: 45,847,462-45,881,921 , GRCh37.p13 chr19: 46,350,720-46,385,179 FOXA3, IRF2BP1, 1 more genes
    nsv5285994copy number variation1nstd204human GRCh38.p13 chr19: 45,831,442-45,833,591 , GRCh37.p13 chr19: 46,334,700-46,336,849 SYMPK
    nsv5284106copy number variation1nstd204human GRCh38.p13 chr19: 45,776,401-45,855,800 , GRCh37.p13 chr19: 46,279,659-46,359,058 RSPH6A, DMWD, 2 more genes
    nsv5283399copy number variation1nstd204human GRCh38.p13 chr19: 45,827,571-45,830,470 , GRCh37.p13 chr19: 46,330,829-46,333,728 SYMPK
    nsv5020723copy number variation1nstd200human GRCh38 chr19: 45,844,619-45,846,246 , GRCh37.p13 chr19: 46,347,877-46,349,504 SYMPK
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