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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5896730copy number variation1nstd209human GRCh38 chr3: 172,794,819-172,794,904 , GRCh37.p13 chr3: 172,512,609-172,512,694 RNU4-4P, ECT2
    nsv5896500copy number variation1nstd209human GRCh38 chr3: 171,525,972-180,293,041 , GRCh37.p13 chr3: 171,243,761-180,010,829 , RNU6-1120P, 95 more genes
    nsv5675798mobile element insertion2nstd211human GRCh38 chr3: 172,751,590-172,751,590 , GRCh37.p13 chr3: 172,469,380-172,469,380 ECT2
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5402405mobile element insertion1nstd206human GRCh38 chr3: 172,751,590-172,751,641 , GRCh37.p13 chr3: 172,469,380-172,469,431 ECT2
    nsv5367197translocation1nstd200human GRCh38 chr3: 172,841,332-172,841,332 , GRCh38 chr3: 172,820,531-172,820,531 , GRCh37.p13 chr3: 172,538,321-172,538,321 , GRCh37.p13 chr3: 172,559,122-172,559,122 ECT2
    nsv5335814translocation1nstd200human GRCh37 chr3: 172,538,321-172,538,321 , GRCh37 chr3: 172,559,122-172,559,122 , GRCh38.p12 chr3: 172,820,531-172,820,531 , GRCh38.p12 chr3: 172,841,332-172,841,332 ECT2
    nsv5231885copy number variation1nstd204human GRCh38.p13 chr3: 172,818,101-172,823,600 , GRCh37.p13 chr3: 172,535,891-172,541,390 ECT2
    nsv5085931mobile element insertion1nstd203human GRCh38 chr3: 172,751,575-172,751,590 , GRCh37.p13 chr3: 172,469,365-172,469,380 ECT2
    nsv5033132inversion1nstd200human GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130 , LOC105374154, 433 more genes
    nsv4924853copy number variation1nstd200human GRCh38 chr3: 172,759,024-172,759,385 , GRCh37.p13 chr3: 172,476,814-172,477,175 ECT2
    nsv4924852copy number variation1nstd200human GRCh38 chr3: 172,753,459-172,806,727 , GRCh37.p13 chr3: 172,471,249-172,524,517 RNU4-4P, ECT2
    nsv4920742copy number variation1nstd200human GRCh38 chr3: 172,829,762-172,836,685 , GRCh37.p13 chr3: 172,547,552-172,554,475 ECT2
    nsv4728220copy number variation1nstd102humanUncertain significance GRCh37 chr3: 172,521,399-172,794,826 , GRCh38.p12 chr3: 172,803,609-173,077,036 SPATA16, ATP5MC1P4, 3 more genes
    nsv4674680copy number variation1nstd102humanPathogenic GRCh37 chr3: 169,617,690-190,593,854 , GRCh38.p12 chr3: 169,899,902-190,876,065 RNU6-1120P, LOC105374262, 323 more genes
    nsv4661857copy number variation1nstd186human GRCh37 chr3: 172,538,217-172,538,403 , GRCh38.p12 chr3: 172,820,427-172,820,613 ECT2
    nsv4596221copy number variation2nstd183human GRCh37 chr3: 172,538,217-172,538,403 , GRCh38.p12 chr3: 172,820,427-172,820,613 ECT2
    nsv4585387copy number variation1nstd183human GRCh37 chr3: 172,537,871-172,538,403 , GRCh38.p12 chr3: 172,820,081-172,820,613 ECT2
    nsv4585386copy number variation1nstd183human GRCh37 chr3: 172,536,713-172,538,668 , GRCh38.p12 chr3: 172,818,923-172,820,878 ECT2
    nsv4562356mobile element insertion1nstd166human GRCh37.p13 chr3: 172,510,301-172,510,301 , GRCh38.p12 chr3: 172,792,511-172,792,511 ECT2
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