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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148254copy number variation1nstd102humanPathogenic GRCh38 chr17: 165,730-11,404,096 , GRCh37.p13 chr17: 396,627-11,307,413 RFLNB, C17orf100, 401 more genes
    nsv7073912inversion1nstd229human GRCh38 chr17: 1,213,690-8,318,220 , GRCh37.p13 chr17: 1,116,984-8,221,538 TNFSF12, SCARNA21, 321 more genes
    nsv7073657inversion1nstd229human GRCh38 chr17: 3,848,628-8,774,303 , GRCh37.p13 chr17: 3,751,922-8,677,621 LOC107987245, TRI-AAT5-5, 243 more genes
    nsv7068795inversion1nstd229human GRCh38 chr17: 4,882,859-5,367,549 , GRCh37.p13 chr17: 4,786,154-5,270,844 CAMTA2, LOC105371505, 27 more genes
    nsv7066143inversion1nstd229human GRCh38 chr17: 4,866,113-4,876,883 , GRCh37.p13 chr17: 4,769,408-4,780,178 MINK1
    nsv6995854copy number variation1nstd229human GRCh38 chr17: 4,866,201-4,872,800 , GRCh37.p13 chr17: 4,769,496-4,776,095 MINK1
    nsv6992814copy number variation1nstd229human GRCh38 chr17: 4,870,001-4,876,900 , GRCh37.p13 chr17: 4,773,296-4,780,195 MINK1
    nsv6992799copy number variation1nstd229human GRCh38 chr17: 4,703,601-4,840,000 , GRCh37.p13 chr17: 4,606,896-4,743,295 RPS12P29, PELP1-DT, 11 more genes
    nsv6991124copy number variation1nstd229human GRCh38 chr17: 4,897,777-4,900,911 , GRCh37.p13 chr17: 4,801,072-4,804,206 C17orf107, MINK1, 1 more genes
    nsv6985628copy number variation1nstd229human GRCh38 chr17: 4,867,448-4,906,651 , GRCh37.p13 chr17: 4,770,743-4,809,946 CHRNE, MINK1, 2 more genes
    nsv6983397copy number variation1nstd229human GRCh38 chr17: 4,870,163-4,876,883 , GRCh37.p13 chr17: 4,773,458-4,780,178 MINK1
    nsv6983269copy number variation1nstd229human GRCh38 chr17: 4,847,928-4,855,509 , GRCh37.p13 chr17: 4,751,223-4,758,804 ATP6V0CP1, MINK1
    nsv6982942copy number variation1nstd229human GRCh38 chr17: 4,854,758-4,859,067 , GRCh37.p13 chr17: 4,758,053-4,762,362 ATP6V0CP1, MINK1
    nsv6982770copy number variation1nstd229human GRCh38 chr17: 3,468,201-5,384,400 , GRCh37.p13 chr17: 3,371,495-5,287,720 SLC25A11, CAMKK1, 83 more genes
    nsv6982450copy number variation1nstd229human GRCh38 chr17: 1,838,614-7,660,509 , GRCh37.p13 chr17: 1,741,908-7,563,827 NCBP3, OR1P1, 242 more genes
    nsv6980084copy number variation1nstd229human GRCh38 chr17: 4,886,556-4,886,674 , GRCh37.p13 chr17: 4,789,851-4,789,969 MINK1
    nsv6979903copy number variation1nstd229human GRCh38 chr17: 4,825,063-4,835,222 , GRCh37.p13 chr17: 4,728,358-4,738,517 MINK1
    nsv6979592copy number variation1nstd229human GRCh38 chr17: 4,273,434-4,887,250 , GRCh37.p13 chr17: 4,176,729-4,790,545 PELP1-DT, RPS12P29, 28 more genes
    nsv6978631copy number variation1nstd229human GRCh38 chr17: 4,870,107-4,876,883 , GRCh37.p13 chr17: 4,773,402-4,780,178 MINK1
    nsv6638055copy number variation1nstd102humanUncertain significance GRCh37 chr17: 4,658,216-5,266,343 , GRCh38.p12 chr17: 4,754,921-5,363,048 RABEP1, SLC25A11, 33 more genes
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