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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5941541copy number variation1nstd209human GRCh38 chr17: 40,126,632-40,126,887 , GRCh37.p13 chr17: 38,282,885-38,283,140 MSL1
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5530898copy number variation1nstd206human GRCh38 chr17: 40,132,334-40,132,388 , GRCh37.p13 chr17: 38,288,587-38,288,641 MSL1
    nsv5367190translocation1nstd200human GRCh38 chr3: 170,788,402-170,788,402 , GRCh38 chr17: 40,136,391-40,136,391 , GRCh37.p13 chr17: 38,292,644-38,292,644 , GRCh37.p13 chr3: 170,506,191-170,506,191 LOC105374211, MSL1
    nsv5298516copy number variation1nstd204human GRCh37.p13 chr17: 38,275,054-38,378,452 , GRCh38.p13 chr17: 40,118,801-40,222,200 CASC3, RAPGEFL1, 4 more genes
    nsv5283669copy number variation1nstd204human GRCh38.p13 chr17: 39,851,001-40,379,500 , GRCh37.p13 chr17: 38,007,254-38,535,752 , CASC3, 27 more genes
    nsv5016317copy number variation1nstd200human GRCh38 chr17: 40,126,632-40,126,888 , GRCh37.p13 chr17: 38,282,885-38,283,141 MSL1
    nsv5016316copy number variation1nstd200human GRCh38 chr17: 40,120,940-40,121,453 , GRCh37.p13 chr17: 38,277,193-38,277,706 MSL1
    nsv5013690copy number variation1nstd200human GRCh38 chr17: 40,127,824-40,138,078 , GRCh37.p13 chr17: 38,284,077-38,294,331 MSL1
    nsv4858786copy number variation1nstd200human GRCh37 chr17: 38,282,885-38,283,141 , GRCh38.p12 chr17: 40,126,632-40,126,888 MSL1
    nsv4858785copy number variation1nstd200human GRCh37 chr17: 38,277,193-38,277,706 , GRCh38.p12 chr17: 40,120,940-40,121,453 MSL1
    nsv4628986copy number variation1nstd183human GRCh37 chr17: 38,215,916-38,530,107 , GRCh38.p12 chr17: 40,059,663-40,373,855 PPIAP54, MSL1, 14 more genes
    nsv4531327copy number variation1nstd166human GRCh37.p13 chr17: 38,290,153-38,290,531 , GRCh38.p12 chr17: 40,133,900-40,134,278 MSL1
    nsv4457831copy number variation1nstd102humanPathogenic GRCh37 chr17: 21,690,653-38,772,647 , GRCh38.p12 chr17: 22,164,047-40,616,395 LOC105371753, TAOK1, 474 more genes
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4271309copy number variation1nstd166human GRCh37.p13 chr17: 38,288,587-38,288,651 , GRCh38.p12 chr17: 40,132,334-40,132,398 MSL1
    nsv4256840copy number variation1nstd166human GRCh37.p13 chr17: 38,282,885-38,283,141 , GRCh38.p12 chr17: 40,126,632-40,126,888 MSL1
    nsv4253892copy number variation1nstd166human GRCh37.p13 chr17: 38,289,911-38,290,078 , GRCh38.p12 chr17: 40,133,658-40,133,825 MSL1
    nsv3914783copy number variation1nstd102humanPathogenic NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577 LOC105371922, GJD3, 1855 more genes
    nsv3913552copy number variation1nstd102humanPathogenic GRCh38 chr17: 36,449,220-75,053,130 , NCBI36 chr17: 54,950,518-70,560,820 , GRCh37 chr17: 57,595,736-73,049,225 RNU6-131P, ZNF652, 1075 more genes
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