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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145597copy number variation1nstd232human GRCh37.p13 chr17: 42,293,177-42,293,272 , GRCh38.p12 chr17: 44,215,809-44,215,904 UBTF, ATXN7L3-AS1
    nsv7145416copy number variation1nstd232human GRCh37.p13 chr17: 42,287,602-42,287,684 , GRCh38.p12 chr17: 44,210,234-44,210,316 UBTF, ATXN7L3-AS1
    nsv7143925copy number variation1nstd232human GRCh37.p13 chr17: 42,284,735-42,284,820 , GRCh38.p12 chr17: 44,207,367-44,207,452 UBTF, ATXN7L3-AS1, 1 more genes
    nsv6992489copy number variation1nstd229human GRCh38 chr17: 44,199,901-44,221,400 , GRCh37.p13 chr17: 42,277,269-42,298,768 UBTF, ATXN7L3-AS1, 1 more genes
    nsv6982861copy number variation1nstd229human GRCh38 chr17: 38,291,672-47,498,259 , GRCh37.p13 chr17: 36,510,266-45,575,625 KRT20, PLEKHH3, 442 more genes
    nsv6496821copy number variation1nstd223human GRCh38 chr17: 44,200,725-44,203,226 , GRCh37.p13 chr17: 42,278,093-42,280,594 UBTF, ATXN7L3-AS1
    nsv6496529copy number variation1nstd223human GRCh38 chr17: 44,218,101-44,224,900 , GRCh37.p13 chr17: 42,295,469-42,302,268 UBTF, ATXN7L3-AS1
    nsv6291646copy number variation1nstd102humanUncertain significance GRCh37 chr17: 42,085,508-42,361,563 , GRCh38.p12 chr17: 44,008,140-44,284,195 LOC105371790, HDAC5, 16 more genes
    nsv6133311copy number variation3nstd213human GRCh37 chr17: 41,970,000-42,760,001 , GRCh38.p12 chr17: 43,892,632-44,682,633 FZD2, GRN, 43 more genes
    nsv5939876copy number variation1nstd209human GRCh38 chr17: 44,204,385-44,204,440 , GRCh37.p13 chr17: 42,281,753-42,281,808 UBTF, ATXN7L3-AS1
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5358884translocation1nstd200human GRCh38 chr17: 44,220,047-44,220,047 , GRCh38 chr17: 44,220,126-44,220,126 , GRCh37.p13 chr17: 42,297,415-42,297,415 , GRCh37.p13 chr17: 42,297,494-42,297,494 ATXN7L3-AS1, UBTF
    nsv5293690copy number variation1nstd204human GRCh37.p13 chr17: 42,260,169-42,295,568 , GRCh38.p13 chr17: 44,182,801-44,218,200 UBTF, ATXN7L3, 4 more genes
    nsv5281720copy number variation1nstd204human GRCh38.p13 chr17: 44,221,501-44,251,800 , GRCh37.p13 chr17: 42,298,869-42,329,168 UBTF, ATXN7L3-AS1, 2 more genes
    nsv5016514copy number variation1nstd200human GRCh38 chr17: 44,200,725-44,203,226 , GRCh37.p13 chr17: 42,278,093-42,280,594 UBTF, ATXN7L3-AS1
    nsv4681862copy number variation1nstd102humanUncertain significance GRCh37 chr17: 42,105,175-42,430,244 , GRCh38.p12 chr17: 44,027,807-44,352,876 G6PC3, ATXN7L3, 21 more genes
    nsv4634035copy number variation1nstd183human GRCh37 chr17: 42,295,633-42,298,989 , GRCh38.p12 chr17: 44,218,265-44,221,621 UBTF, ATXN7L3-AS1
    nsv4503618mobile element insertion1nstd166human GRCh37.p13 chr17: 42,282,557-42,282,557 , GRCh38.p12 chr17: 44,205,189-44,205,189 ATXN7L3-AS1, UBTF
    nsv4422397copy number variation1nstd174human GRCh37 chr17: 42,295,583-42,299,041 , GRCh38.p12 chr17: 44,218,215-44,221,673 ATXN7L3-AS1, UBTF
    nsv4370994copy number variation1nstd173human GRCh37 chr17: 42,204,597-42,399,013 , GRCh38.p12 chr17: 44,127,229-44,321,645 RNU6-453P, RN7SL507P, 15 more genes
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