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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6127764copy number variation1nstd186human GRCh37 chr17: 35,778,706-35,782,390 , GRCh38.p12 chr17: 37,418,621-37,422,284 , GRCh38.p12 chr17|NT_187614.1: 1,657,771-1,661,455 TADA2A
    nsv6125591copy number variation1nstd186human GRCh37 chr17: 35,796,584-35,797,613 , GRCh38.p12 chr17: 37,436,483-37,437,512 , GRCh38.p12 chr17|NT_187614.1: 1,675,649-1,676,678 TADA2A
    nsv6112791copy number variation1nstd102humanPathogenic GRCh37 chr17: 34,815,466-36,249,366 , GRCh38.p12 chr17|NT_187614.1: 694,556-2,128,431 , GRCh38.p12 chr17: 36,459,652-37,889,744 HNF1B, LOC107985031, 36 more genes
    nsv5967562inversion1nstd209human GRCh38 chr17: 37,415,697-37,416,258 , GRCh37.p13 chr17: 35,775,781-35,776,343 TADA2A
    nsv5944046copy number variation1nstd209human GRCh38 chr17: 37,436,483-37,437,511 , GRCh37.p13 chr17: 35,796,584-35,797,612 TADA2A
    nsv5940835copy number variation1nstd209human GRCh38 chr17: 37,464,561-37,464,867 , GRCh37.p13 chr17: 35,824,665-35,824,971 TADA2A
    nsv5937630copy number variation1nstd209human GRCh38 chr17: 37,418,845-37,422,299 , GRCh37.p13 chr17: 35,778,929-35,782,405 TADA2A
    nsv5932561copy number variation1nstd209human GRCh38 chr17: 36,271,341-37,995,711 , GRCh37.p13 chr17: 34,900,240-35,888,667 LOC101060212, RNU6-1192P, 47 more genes
    nsv5887122copy number variation1nstd209human GRCh38 chr17: 37,436,443-37,437,556 , GRCh37.p13 chr17: 35,796,544-35,797,657 TADA2A
    nsv5873656copy number variation1nstd209human GRCh38 chr17: 37,418,929-37,422,228 , GRCh37.p13 chr17: 35,779,013-35,782,334 TADA2A
    nsv5716593mobile element insertion2nstd211human GRCh38 chr17: 37,460,084-37,460,084 , GRCh37.p13 chr17: 35,820,188-35,820,188 TADA2A
    nsv5710514mobile element insertion1nstd211human GRCh38 chr17: 37,432,952-37,432,952 , GRCh37.p13 chr17: 35,793,052-35,793,052 TADA2A
    nsv5707775mobile element insertion2nstd211human GRCh38 chr17: 37,436,792-37,436,792 , GRCh37.p13 chr17: 35,796,893-35,796,893 TADA2A
    nsv5665268inversion1nstd207human GRCh37.p13 chr17: 35,775,175-35,775,781 , GRCh38 chr17: 37,415,091-37,415,697 TADA2A
    nsv5601094copy number variation1nstd207human GRCh38 chr17: 37,415,232-37,415,584 , GRCh37.p13 chr17: 35,775,316-35,775,668 TADA2A
    nsv5600099copy number variation1nstd207human GRCh38 chr17: 37,415,641-37,415,694 , GRCh37.p13 chr17: 35,775,725-35,775,778 TADA2A
    nsv5594240copy number variation1nstd207human GRCh38 chr17: 37,418,845-37,422,299 , GRCh37.p13 chr17: 35,778,929-35,782,405 TADA2A
    nsv5585964copy number variation1nstd207human GRCh38 chr17: 37,436,483-37,437,510 , GRCh37.p13 chr17: 35,796,584-35,797,611 TADA2A
    nsv5557179inversion1nstd206human GRCh38 chr17: 37,415,128-37,415,701 , GRCh37.p13 chr17: 35,775,212-35,775,785 TADA2A
    nsv5556879sequence alteration1nstd206human GRCh38 chr17: 37,453,907-37,453,946 , GRCh37.p13 chr17: 35,814,009-35,814,048 TADA2A, LOC100419621
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