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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137724copy number variation1nstd102humanPathogenic GRCh37 chr1: 16,785,250-23,491,592 , GRCh38.p12 chr1: 16,458,755-23,165,099 PADI1, RPS15AP6, 176 more genes
    nsv5878618copy number variation1nstd209human GRCh38 chr1: 21,967,428-21,993,097 , GRCh37.p13 chr1: 22,293,921-22,319,590 CELA3B, RN7SL386P, 1 more genes
    nsv5875729copy number variation1nstd209human GRCh38 chr1: 21,981,207-22,005,757 , GRCh37.p13 chr1: 22,307,700-22,332,250 CELA3A, CELA3B, 2 more genes
    nsv5872010copy number variation1nstd209human GRCh38 chr1: 21,985,867-22,008,697 , GRCh37.p13 chr1: 22,312,360-22,335,190 CELA3A, CELA3B, 3 more genes
    nsv5829443copy number variation2nstd209human GRCh38 chr1: 21,980,341-21,985,173 , GRCh37.p13 chr1: 22,306,834-22,311,666 CELA3B
    nsv5829361copy number variation2nstd209human GRCh38 chr1: 21,967,929-21,979,206 , GRCh37.p13 chr1: 22,294,422-22,305,699 CELA3B
    nsv5828903copy number variation2nstd209human GRCh38 chr1: 21,989,654-21,993,098 , GRCh37.p13 chr1: 22,316,147-22,319,591 CELA3B
    nsv5610648insertion1nstd207human GRCh38 chr1: 21,986,212-21,986,212 , GRCh37.p13 chr1: 22,312,705-22,312,705 CELA3B, RN7SL386P, 1 more genes
    nsv5583738copy number variation1nstd207human GRCh38 chr1: 21,969,930-21,995,605 , GRCh37.p13 chr1: 22,296,423-22,322,098 CELA3B, RN7SL386P, 1 more genes
    nsv5571711copy number variation1nstd207human GRCh38 chr1: 21,967,354-21,979,656 , GRCh37.p13 chr1: 22,293,847-22,306,149 CELA3B
    nsv5433283copy number variation1nstd206human GRCh38 chr1: 21,983,081-22,008,663 , GRCh37.p13 chr1: 22,309,574-22,335,156 RN7SL186P, RN7SL386P, 3 more genes
    nsv5420965copy number variation1nstd206human GRCh38 chr1: 21,979,163-22,005,163 , GRCh37.p13 chr1: 22,305,656-22,331,656 CELA3A, RN7SL386P, 2 more genes
    nsv5365457translocation1nstd200human GRCh38 chr1: 21,986,165-21,986,165 , GRCh38 chr1: 22,064,870-22,064,870 , GRCh37.p13 chr1: 22,312,658-22,312,658 , GRCh37.p13 chr1: 22,391,363-22,391,363 CDC42, CELA3B, 2 more genes
    nsv5286250copy number variation1nstd204human GRCh38.p13 chr1: 21,981,911-21,982,882 , GRCh37.p13 chr1: 22,308,404-22,309,375 CELA3B
    nsv5220240copy number variation1nstd204human GRCh38.p13 chr1: 21,967,929-21,976,161 , GRCh37.p13 chr1: 22,294,422-22,302,654 CELA3B
    nsv5219149copy number variation1nstd204human GRCh38.p13 chr1: 21,968,201-21,977,700 , GRCh37.p13 chr1: 22,294,694-22,304,193 CELA3B
    nsv5218269copy number variation1nstd204human GRCh38.p13 chr1: 21,988,101-21,990,400 , GRCh37.p13 chr1: 22,314,594-22,316,893 RNU6-1022P, RN7SL386P, 1 more genes
    nsv5216220copy number variation1nstd204human GRCh38.p13 chr1: 21,978,448-21,980,590 , GRCh37.p13 chr1: 22,304,941-22,307,083 CELA3B
    nsv5214003copy number variation1nstd204human GRCh37.p13 chr1: 22,314,494-22,338,993 , GRCh38.p13 chr1: 21,988,001-22,012,500 CELA3A, CELA3B, 4 more genes
    nsv5213128copy number variation1nstd204human GRCh38.p13 chr1: 21,981,232-21,982,680 , GRCh37.p13 chr1: 22,307,725-22,309,173 CELA3B
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