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Items: 1 to 20 of 293

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5930760copy number variation1nstd209human GRCh38 chr17: 4,854,754-4,859,065 , GRCh37.p13 chr17: 4,758,049-4,762,360 MINK1, ATP6V0CP1
    nsv5886517copy number variation1nstd209human GRCh38 chr17: 4,870,155-4,871,975 , GRCh37.p13 chr17: 4,773,450-4,775,270 MINK1
    nsv5869713copy number variation1nstd209human GRCh38 chr17: 4,854,730-4,858,979 , GRCh37.p13 chr17: 4,758,025-4,762,274 MINK1, ATP6V0CP1
    nsv5869118copy number variation1nstd209human GRCh38 chr17: 4,870,576-4,876,404 , GRCh37.p13 chr17: 4,773,871-4,779,699 MINK1
    nsv5663324insertion1nstd207human GRCh38 chr17: 4,879,200-4,879,200 , GRCh37.p13 chr17: 4,782,495-4,782,495 MINK1
    nsv5650807insertion1nstd207human GRCh38 chr17: 4,852,769-4,852,769 , GRCh37.p13 chr17: 4,756,064-4,756,064 MINK1
    nsv5648861insertion1nstd207human GRCh38 chr17: 4,870,378-4,870,378 , GRCh37.p13 chr17: 4,773,673-4,773,673 MINK1
    nsv5589404copy number variation1nstd207human GRCh38 chr17: 4,878,998-4,879,053 , GRCh37.p13 chr17: 4,782,293-4,782,348 MINK1
    nsv5586692copy number variation1nstd207human GRCh38 chr17: 4,879,032-4,879,144 , GRCh37.p13 chr17: 4,782,327-4,782,439 MINK1
    nsv5563101sequence alteration1nstd206human GRCh38 chr17: 4,866,112-4,876,882 , GRCh37.p13 chr17: 4,769,407-4,780,177 MINK1
    nsv5532963copy number variation1nstd206human GRCh38 chr17: 4,869,111-4,877,111 , GRCh37.p13 chr17: 4,772,406-4,780,406 MINK1
    nsv5527586copy number variation1nstd206human GRCh38 chr17: 4,854,757-4,859,066 , GRCh37.p13 chr17: 4,758,052-4,762,361 ATP6V0CP1, MINK1
    nsv5515835copy number variation1nstd206human GRCh38 chr17: 4,869,513-4,869,771 , GRCh37.p13 chr17: 4,772,808-4,773,066 MINK1
    nsv5358586translocation1nstd200human GRCh38 chr17: 4,854,757-4,854,757 , GRCh38 chr17: 4,859,066-4,859,066 , GRCh37.p13 chr17: 4,762,361-4,762,361 , GRCh37.p13 chr17: 4,758,052-4,758,052 MINK1
    nsv5295114copy number variation1nstd204human GRCh38.p13 chr17: 4,830,401-4,832,300 , GRCh37.p13 chr17: 4,733,696-4,735,595 MINK1
    nsv5283967copy number variation1nstd204human GRCh38.p13 chr17: 4,830,501-5,066,500 , GRCh37.p13 chr17: 4,733,796-4,969,795 , RN7SL784P, 20 more genes
    nsv5015604copy number variation1nstd200human GRCh38 chr17: 4,883,700-4,883,756 , GRCh37.p13 chr17: 4,786,995-4,787,051 MINK1, RN7SL784P
    nsv5015603copy number variation1nstd200human GRCh38 chr17: 4,869,513-4,869,771 , GRCh37.p13 chr17: 4,772,808-4,773,066 MINK1
    nsv4864479copy number variation1nstd200human GRCh37 chr17: 4,687,640-4,824,332 , GRCh38.p12 chr17: 4,784,345-4,921,037 CHRNE, PLD2, 7 more genes
    nsv4857831copy number variation1nstd200human GRCh37 chr17: 4,758,052-4,762,361 , GRCh38.p12 chr17: 4,854,757-4,859,066 MINK1, ATP6V0CP1
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