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Items: 1 to 20 of 238

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5920648copy number variation1nstd209human GRCh38 chr10: 18,009,336-18,009,401 , GRCh37.p13 chr10: 18,298,265-18,298,330 SLC39A12-AS1, SLC39A12
    nsv5634906insertion1nstd207human GRCh38 chr10: 17,971,268-17,971,268 , GRCh37.p13 chr10: 18,260,197-18,260,197 SLC39A12
    nsv5629973insertion1nstd207human GRCh38 chr10: 17,950,559-17,950,559 , GRCh37.p13 chr10|NW_003315932.1: 379,350-379,350 , GRCh37.p13 chr10: 18,239,488-18,239,488 SLC39A12
    nsv5628827insertion1nstd207human GRCh38 chr10: 18,041,721-18,041,721 , GRCh37.p13 chr10: 18,330,650-18,330,650 SLC39A12
    nsv5594097copy number variation1nstd207human GRCh38 chr10: 18,041,591-18,041,654 , GRCh37.p13 chr10: 18,330,520-18,330,583 SLC39A12
    nsv5539374insertion1nstd206human GRCh38 chr10: 17,950,559-17,950,559 , GRCh37.p13 chr10: 18,239,488-18,239,488 , GRCh37.p13 chr10|NW_003315932.1: 379,350-379,350 SLC39A12
    nsv5485307copy number variation1nstd206human GRCh38 chr10: 17,969,293-17,969,347 , GRCh37.p13 chr10: 18,258,222-18,258,276 SLC39A12
    nsv5341947translocation1nstd200human GRCh37 chr10: 18,298,267-18,298,267 , GRCh37 chr10: 18,298,331-18,298,331 , GRCh38.p12 chr10: 18,009,402-18,009,402 , GRCh38.p12 chr10: 18,009,338-18,009,338 SLC39A12, SLC39A12-AS1
    nsv5247868copy number variation1nstd204human GRCh38.p13 chr10: 18,036,927-18,072,215 , GRCh37.p13 chr10: 18,325,856-18,361,144 SLC39A12
    nsv5130983mobile element insertion1nstd203human GRCh38 chr10: 17,973,587-17,973,602 , GRCh37.p13 chr10: 18,262,516-18,262,531 SLC39A12
    nsv5122665mobile element insertion1nstd203human GRCh38 chr10: 17,957,120-17,957,134 , GRCh37.p13 chr10: 18,246,049-18,246,063 , GRCh37.p13 chr10|NW_003315932.1: 385,911-385,925 SLC39A12
    nsv4975195copy number variation1nstd200human GRCh38 chr10: 17,982,524-17,986,731 , GRCh37.p13 chr10: 18,271,453-18,275,660 SLC39A12
    nsv4975194copy number variation1nstd200human GRCh38 chr10: 17,971,255-17,974,111 , GRCh37.p13 chr10: 18,260,184-18,263,040 SLC39A12
    nsv4975193copy number variation1nstd200human GRCh38 chr10: 17,969,293-17,969,347 , GRCh37.p13 chr10: 18,258,222-18,258,276 SLC39A12
    nsv4975192copy number variation1nstd200human GRCh38 chr10: 17,948,674-17,954,611 , GRCh37.p13 chr10|NW_003315932.1: 377,465-383,402 , GRCh37.p13 chr10: 18,237,603-18,243,540 SLC39A12
    nsv4845733copy number variation1nstd200human GRCh37 chr10: 18,271,453-18,275,660 , GRCh38.p12 chr10: 17,982,524-17,986,731 SLC39A12
    nsv4750927insertion1nstd199human GRCh37 chr10: 18,239,476-18,239,476 , GRCh38.p12 chr10: 17,950,547-17,950,547 SLC39A12
    nsv4746309copy number variation1nstd199human GRCh37 chr10: 18,330,555-18,330,619 , GRCh38.p12 chr10: 18,041,626-18,041,690 SLC39A12
    nsv4729684copy number variation1nstd102humanUncertain significance GRCh37 chr10: 18,313,841-18,388,434 , GRCh38.p12 chr10: 18,024,912-18,099,505 SLC39A12
    nsv4723144mobile element insertion1nstd186human GRCh37 chr10: 18,325,695-18,325,695 , GRCh38.p12 chr10: 18,036,766-18,036,766 SLC39A12
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