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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6121608copy number variation1nstd186human GRCh37 chr12: 112,027,416-112,027,631 , GRCh38.p12 chr12: 111,589,612-111,589,827 ATXN2
    nsv6121120copy number variation1nstd186human GRCh37 chr12: 111,976,294-111,980,008 , GRCh38.p12 chr12: 111,538,490-111,542,204 ATXN2
    nsv5973958inversion1nstd209human GRCh38 chr12: 111,582,993-111,583,782 , GRCh37.p13 chr12: 112,020,797-112,021,586 ATXN2
    nsv5969388inversion1nstd209human GRCh38 chr12: 111,538,479-111,542,193 , GRCh37.p13 chr12: 111,976,283-111,979,997 ATXN2
    nsv5945497copy number variation1nstd209human GRCh38 chr12: 111,538,508-111,542,254 , GRCh37.p13 chr12: 111,976,312-111,980,058 ATXN2
    nsv5938874copy number variation1nstd209human GRCh38 chr12: 111,459,510-111,460,150 , GRCh37.p13 chr12: 111,897,314-111,897,954 ATXN2
    nsv5933287copy number variation1nstd209human GRCh38 chr12: 111,595,797-111,595,934 , GRCh37.p13 chr12: 112,033,601-112,033,738 ATXN2
    nsv5932171copy number variation1nstd209human GRCh38 chr12: 111,532,770-111,537,889 , GRCh37.p13 chr12: 111,970,574-111,975,693 ATXN2
    nsv5929814copy number variation1nstd209human GRCh38 chr12: 111,575,130-111,589,733 , GRCh37.p13 chr12: 112,012,934-112,027,537 ATXN2, IFITM3P5
    nsv5928538copy number variation1nstd209human GRCh38 chr12: 111,589,649-111,590,090 , GRCh37.p13 chr12: 112,027,453-112,027,894 ATXN2
    nsv5861183copy number variation2nstd209human GRCh38 chr12: 111,584,360-111,589,894 , GRCh37.p13 chr12: 112,022,164-112,027,698 ATXN2
    nsv5859874copy number variation1nstd209human GRCh38 chr12: 111,575,085-111,582,709 , GRCh37.p13 chr12: 112,012,889-112,020,513 IFITM3P5, ATXN2
    nsv5858502copy number variation1nstd209human GRCh38 chr12: 111,538,427-111,541,312 , GRCh37.p13 chr12: 111,976,231-111,979,116 ATXN2
    nsv5854260copy number variation1nstd209human GRCh38 chr12: 111,526,009-111,527,211 , GRCh37.p13 chr12: 111,963,813-111,965,015 ATXN2
    nsv5853940copy number variation1nstd209human GRCh38 chr12: 111,534,043-111,537,326 , GRCh37.p13 chr12: 111,971,847-111,975,130 ATXN2
    nsv5727200mobile element insertion1nstd211human GRCh38 chr12: 111,587,336-111,587,336 , GRCh37.p13 chr12: 112,025,140-112,025,140 ATXN2
    nsv5698438mobile element insertion2nstd211human GRCh38 chr12: 111,534,609-111,534,609 , GRCh37.p13 chr12: 111,972,413-111,972,413 ATXN2
    nsv5696781mobile element insertion1nstd211human GRCh38 chr12: 111,529,428-111,529,428 , GRCh37.p13 chr12: 111,967,232-111,967,232 ATXN2
    nsv5662324insertion1nstd207human GRCh38 chr12: 111,589,649-111,589,649 , GRCh37.p13 chr12: 112,027,453-112,027,453 ATXN2
    nsv5589992copy number variation1nstd207human GRCh38 chr12: 111,595,797-111,595,934 , GRCh37.p13 chr12: 112,033,601-112,033,738 ATXN2
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