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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5953441insertion1nstd209human GRCh38 chr3: 112,205,624-112,205,624 , GRCh37.p13 chr3: 111,924,471-111,924,471 SLC9C1
    nsv5898352copy number variation1nstd209human GRCh38 chr3: 112,201,698-112,201,893 , GRCh37.p13 chr3: 111,920,545-111,920,740 SLC9C1
    nsv5728605mobile element insertion1nstd211human GRCh38 chr3: 112,208,798-112,208,798 , GRCh37.p13 chr3: 111,927,645-111,927,645 SLC9C1
    nsv5679141mobile element insertion2nstd211human GRCh38 chr3: 112,294,742-112,294,742 , GRCh37.p13 chr3: 112,013,589-112,013,589 SLC9C1
    nsv5617508insertion1nstd207human GRCh38 chr3: 112,164,434-112,164,434 , GRCh37.p13 chr3: 111,883,281-111,883,281 SLC9C1
    nsv5610731insertion1nstd207human GRCh38 chr3: 112,205,624-112,205,624 , GRCh37.p13 chr3: 111,924,471-111,924,471 SLC9C1
    nsv5442944copy number variation1nstd206human GRCh38 chr3: 112,265,328-112,265,416 , GRCh37.p13 chr3: 111,984,175-111,984,263 SLC9C1
    nsv5407085mobile element insertion1nstd206human GRCh38 chr3: 112,294,742-112,294,793 , GRCh37.p13 chr3: 112,013,589-112,013,640 SLC9C1
    nsv5346412translocation1nstd200human GRCh38 chr3: 112,217,821-112,217,821 , GRCh38 chr3: 112,217,366-112,217,366 , GRCh37.p13 chr3: 111,936,668-111,936,668 , GRCh37.p13 chr3: 111,936,213-111,936,213 SLC9C1
    nsv5302598copy number variation1nstd204human GRCh38.p13 chr3: 109,643,426-112,176,826 , GRCh37.p13 chr3: 109,362,273-111,895,673 , NECTIN3-AS1, 28 more genes
    nsv5235498copy number variation1nstd204human GRCh38.p13 chr3: 112,205,401-112,206,200 , GRCh37.p13 chr3: 111,924,248-111,925,047 SLC9C1
    nsv5229675copy number variation1nstd204human GRCh38.p13 chr3: 111,834,401-112,176,600 , GRCh37.p13 chr3: 111,553,248-111,895,447 TMPRSS7, PLCXD2, 10 more genes
    nsv5099683mobile element insertion1nstd203human GRCh38 chr3: 112,146,271-112,146,285 , GRCh37.p13 chr3: 111,865,118-111,865,132 SLC9C1
    nsv5096817mobile element insertion1nstd203human GRCh38 chr3: 112,224,602-112,224,615 , GRCh37.p13 chr3: 111,943,449-111,943,462 SLC9C1
    nsv5092367mobile element insertion1nstd203human GRCh38 chr3: 112,294,736-112,294,742 , GRCh37.p13 chr3: 112,013,583-112,013,589 SLC9C1
    nsv5088122mobile element insertion1nstd203human GRCh38 chr3: 112,204,772-112,204,781 , GRCh37.p13 chr3: 111,923,619-111,923,628 SLC9C1
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv5031637inversion1nstd200human GRCh38 chr3: 112,181,184-125,673,487 , GRCh37.p13 chr3: 111,900,031-125,392,331 , ARHGAP31, 218 more genes
    nsv4919558copy number variation1nstd200human GRCh38 chr3: 112,238,281-112,257,205 , GRCh37.p13 chr3: 111,957,128-111,976,052 LOC100532749, SLC9C1
    nsv4919557copy number variation1nstd200human GRCh38 chr3: 112,201,698-112,201,894 , GRCh37.p13 chr3: 111,920,545-111,920,741 SLC9C1
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