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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6733093copy number variation1nstd229human GRCh38 chr3: 142,878,081-142,926,071 , GRCh37.p13 chr3: 142,596,923-142,644,913 PCOLCE2, LOC100507389
    nsv6727008copy number variation1nstd229human GRCh38 chr3: 142,255,714-146,323,295 , GRCh37.p13 chr3: 141,974,556-146,041,082 LOC105374142, XRN1, 44 more genes
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6562831inversion1nstd223human GRCh38 chr3: 142,555,219-148,451,915 , GRCh37.p13 chr3: 142,274,061-148,169,702 LOC102724145, PLS1, 60 more genes
    nsv6364047copy number variation1nstd223human GRCh38 chr3: 142,868,501-143,010,800 , GRCh37.p13 chr3: 142,587,343-142,729,642 PCOLCE2, LOC100507389, 4 more genes
    nsv6254773mobile element insertion1nstd215human GRCh38 chr3: 142,932,719-142,932,719 , GRCh37.p13 chr3: 142,651,561-142,651,561 LOC100507389
    nsv6254772mobile element insertion1nstd215human GRCh38 chr3: 142,928,606-142,928,606 , GRCh37.p13 chr3: 142,647,448-142,647,448 LOC100507389
    nsv6134994copy number variation1nstd213human GRCh37 chr3: 139,490,000-150,360,001 , GRCh38.p12 chr3: 139,771,158-150,642,214 , ATP1B3, 147 more genes
    nsv6071234insertion1nstd212human GRCh38 chr3: 142,928,591-142,928,591 , GRCh37.p13 chr3: 142,647,433-142,647,433 LOC100507389
    nsv6064377insertion1nstd212human GRCh38 chr3: 142,932,702-142,932,702 , GRCh37.p13 chr3: 142,651,544-142,651,544 LOC100507389
    nsv5958700insertion1nstd209human GRCh38 chr3: 142,928,591-142,928,591 , GRCh37.p13 chr3: 142,647,433-142,647,433 LOC100507389
    nsv5724625mobile element insertion1nstd211human GRCh38 chr3: 142,932,093-142,932,093 , GRCh37.p13 chr3: 142,650,935-142,650,935 LOC100507389
    nsv5694131mobile element insertion2nstd211human GRCh38 chr3: 142,932,719-142,932,719 , GRCh37.p13 chr3: 142,651,561-142,651,561 LOC100507389
    nsv5693738mobile element insertion2nstd211human GRCh38 chr3: 142,928,606-142,928,606 , GRCh37.p13 chr3: 142,647,448-142,647,448 LOC100507389
    nsv5615827insertion1nstd207human GRCh38 chr3: 142,928,591-142,928,591 , GRCh37.p13 chr3: 142,647,433-142,647,433 LOC100507389
    nsv5561914mobile element insertion1nstd206human GRCh38 chr3: 142,932,107-142,932,144 , GRCh37.p13 chr3: 142,650,949-142,650,986 LOC100507389
    nsv5545082insertion1nstd206human GRCh38 chr3: 142,928,591-142,928,591 , GRCh37.p13 chr3: 142,647,433-142,647,433 LOC100507389
    nsv5410574mobile element insertion1nstd206human GRCh38 chr3: 142,932,719-142,932,770 , GRCh37.p13 chr3: 142,651,561-142,651,612 LOC100507389
    nsv5381765copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,173,683-162,494,699 , GRCh38.p12 chr3: 138,454,841-162,776,911 MBNL1-AS1, LOC107986138, 339 more genes
    nsv5367072translocation1nstd200human GRCh38 chr6: 122,850,243-122,850,243 , GRCh38 chr3: 142,929,757-142,929,757 , GRCh37.p13 chr3: 142,648,599-142,648,599 , GRCh37.p13 chr6: 123,171,388-123,171,388 LOC100507389
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