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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6127661copy number variation1nstd186human GRCh37 chr17: 28,712,364-28,712,601 , GRCh38.p12 chr17: 30,385,346-30,385,583 CPD
    nsv5971581insertion1nstd209human GRCh38 chr17: 30,470,257-30,470,257 , GRCh37.p13 chr17: 28,797,275-28,797,275 CPD
    nsv5936913copy number variation1nstd209human GRCh38 chr17: 30,385,345-30,385,582 , GRCh37.p13 chr17: 28,712,363-28,712,600 CPD
    nsv5935994copy number variation1nstd209human GRCh38 chr17: 30,450,117-30,450,229 , GRCh37.p13 chr17: 28,777,135-28,777,247 CPD
    nsv5723936mobile element insertion1nstd211human GRCh38 chr17: 30,439,376-30,439,376 , GRCh37.p13 chr17: 28,766,394-28,766,394 CPD
    nsv5721983mobile element insertion2nstd211human GRCh38 chr17: 30,397,883-30,397,883 , GRCh37.p13 chr17: 28,724,901-28,724,901 CPD
    nsv5712410mobile element insertion1nstd211human GRCh38 chr17: 30,459,610-30,459,610 , GRCh37.p13 chr17: 28,786,628-28,786,628 CPD
    nsv5703141mobile element insertion2nstd211human GRCh38 chr17: 30,424,117-30,424,117 , GRCh37.p13 chr17: 28,751,135-28,751,135 CPD
    nsv5595929copy number variation1nstd207human GRCh38 chr17: 30,385,345-30,385,582 , GRCh37.p13 chr17: 28,712,363-28,712,600 CPD
    nsv5592840copy number variation1nstd207human GRCh38 chr17: 30,450,117-30,450,229 , GRCh37.p13 chr17: 28,777,135-28,777,247 CPD
    nsv5558881inversion1nstd206human GRCh38 chr17: 30,470,236-30,470,374 , GRCh37.p13 chr17: 28,797,254-28,797,392 CPD
    nsv5555641sequence alteration1nstd206human GRCh38 chr17: 30,429,186-30,435,334 , GRCh37.p13 chr17: 28,756,204-28,762,352 CPD
    nsv5549633insertion1nstd206human GRCh38 chr17: 30,435,318-30,435,318 , GRCh37.p13 chr17: 28,762,336-28,762,336 CPD
    nsv5541014insertion1nstd206human GRCh38 chr17: 30,470,269-30,470,306 , GRCh37.p13 chr17: 28,797,287-28,797,324 CPD
    nsv5535328insertion1nstd206human GRCh38 chr17: 30,459,610-30,459,647 , GRCh37.p13 chr17: 28,786,628-28,786,665 CPD
    nsv5530868copy number variation1nstd206human GRCh38 chr17: 30,462,141-30,462,196 , GRCh37.p13 chr17: 28,789,159-28,789,214 CPD
    nsv5530737copy number variation1nstd206human GRCh38 chr17: 30,450,119-30,450,230 , GRCh37.p13 chr17: 28,777,137-28,777,248 CPD
    nsv5523313copy number variation1nstd206human GRCh38 chr17: 30,385,346-30,385,583 , GRCh37.p13 chr17: 28,712,364-28,712,601 CPD
    nsv5419662mobile element insertion1nstd206human GRCh38 chr17: 30,424,117-30,424,168 , GRCh37.p13 chr17: 28,751,135-28,751,186 CPD
    nsv5358793translocation1nstd200human GRCh38 chr17: 30,385,583-30,385,583 , GRCh38 chr17: 30,385,346-30,385,346 , GRCh37.p13 chr17: 28,712,364-28,712,364 , GRCh37.p13 chr17: 28,712,601-28,712,601 CPD
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