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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5956083insertion1nstd209human GRCh38 chr3: 73,025,574-73,025,574 , GRCh37.p13 chr3: 73,074,725-73,074,725 PPP4R2
    nsv5905009copy number variation1nstd209human GRCh38 chr3: 73,013,926-73,014,402 , GRCh37.p13 chr3: 73,063,077-73,063,553 PPP4R2
    nsv5902904copy number variation1nstd209human GRCh38 chr3: 66,803,410-74,489,186 , GRCh37.p13 chr3: 66,853,834-74,538,337 , LOC105377160, 83 more genes
    nsv5902354copy number variation1nstd209human GRCh38 chr3: 73,031,559-73,032,422 , GRCh37.p13 chr3: 73,080,710-73,081,573 PPP4R2
    nsv5894273copy number variation1nstd209human GRCh38 chr3: 72,995,182-72,996,161 , GRCh37.p13 chr3: 73,044,333-73,045,312 PPP4R2
    nsv5687984mobile element insertion2nstd211human GRCh38 chr3: 73,052,257-73,052,257 , GRCh37.p13 chr3: 73,101,408-73,101,408 PPP4R2
    nsv5684287mobile element insertion1nstd211human GRCh38 chr3: 73,013,214-73,013,214 , GRCh37.p13 chr3: 73,062,365-73,062,365 PPP4R2
    nsv5677825mobile element insertion1nstd211human GRCh38 chr3: 73,025,584-73,025,584 , GRCh37.p13 chr3: 73,074,735-73,074,735 PPP4R2
    nsv5605091insertion1nstd207human GRCh38 chr3: 73,018,452-73,018,452 , GRCh37.p13 chr3: 73,067,603-73,067,603 PPP4R2
    nsv5582704copy number variation1nstd207human GRCh38 chr3: 73,013,926-73,014,402 , GRCh37.p13 chr3: 73,063,077-73,063,553 PPP4R2
    nsv5450701copy number variation1nstd206human GRCh38 chr3: 73,008,773-73,008,857 , GRCh37.p13 chr3: 73,057,924-73,058,008 PPP4R2
    nsv5450456copy number variation1nstd206human GRCh38 chr3: 73,031,559-73,032,424 , GRCh37.p13 chr3: 73,080,710-73,081,575 PPP4R2
    nsv5447363copy number variation1nstd206human GRCh38 chr3: 73,016,065-73,020,345 , GRCh37.p13 chr3: 73,065,216-73,069,496 PPP4R2
    nsv5446519copy number variation1nstd206human GRCh38 chr3: 73,051,487-73,052,585 , GRCh37.p13 chr3: 73,100,638-73,101,736 PPP4R2
    nsv5440176copy number variation1nstd206human GRCh38 chr3: 73,013,518-73,026,685 , GRCh37.p13 chr3: 73,062,669-73,075,836 RNU7-19P, PPP4R2
    nsv5435455copy number variation1nstd206human GRCh38 chr3: 73,013,926-73,014,403 , GRCh37.p13 chr3: 73,063,077-73,063,554 PPP4R2
    nsv5404463mobile element insertion1nstd206human GRCh38 chr3: 73,025,584-73,025,635 , GRCh37.p13 chr3: 73,074,735-73,074,786 PPP4R2
    nsv5398136mobile element insertion1nstd206human GRCh38 chr3: 73,013,214-73,013,265 , GRCh37.p13 chr3: 73,062,365-73,062,416 PPP4R2
    nsv5361661translocation1nstd200human GRCh38 chr3: 73,067,192-73,067,192 , GRCh38 chr19: 36,980,118-36,980,118 , GRCh37.p13 chr19: 37,471,020-37,471,020 , GRCh37.p13 chr3: 73,116,343-73,116,343 ZNF568, PPP4R2
    nsv5361659translocation1nstd200human GRCh38 chr3: 73,008,422-73,008,422 , GRCh38 chr10: 70,688,989-70,688,989 , GRCh37.p13 chr3: 73,057,573-73,057,573 , GRCh37.p13 chr10: 72,448,745-72,448,745 ADAMTS14, PPP4R2
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