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Items: 1 to 20 of 336

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5905908copy number variation1nstd209human GRCh38 chr3: 146,128,715-146,128,775 , GRCh37.p13 chr3: 145,846,502-145,846,562 PLOD2
    nsv5898316copy number variation1nstd209human GRCh38 chr3: 146,148,038-146,148,092 , GRCh37.p13 chr3: 145,865,825-145,865,879 PLOD2
    nsv5677414mobile element insertion2nstd211human GRCh38 chr3: 146,074,387-146,074,387 , GRCh37.p13 chr3: 145,792,174-145,792,174 PLOD2
    nsv5583060copy number variation1nstd207human GRCh38 chr3: 146,128,715-146,128,775 , GRCh37.p13 chr3: 145,846,502-145,846,562 PLOD2
    nsv5449397copy number variation1nstd206human GRCh38 chr3: 146,129,620-146,129,686 , GRCh37.p13 chr3: 145,847,407-145,847,473 PLOD2
    nsv5439732copy number variation1nstd206human GRCh38 chr3: 146,098,709-146,099,309 , GRCh37.p13 chr3: 145,816,496-145,817,096 PLOD2
    nsv5438542copy number variation1nstd206human GRCh38 chr3: 146,157,429-146,157,510 , GRCh37.p13 chr3: 145,875,216-145,875,297 PLOD2
    nsv5437378copy number variation1nstd206human GRCh38 chr3: 146,148,040-146,148,093 , GRCh37.p13 chr3: 145,865,827-145,865,880 PLOD2
    nsv5436305copy number variation1nstd206human GRCh38 chr3: 146,128,722-146,128,776 , GRCh37.p13 chr3: 145,846,509-145,846,563 PLOD2
    nsv5404695mobile element insertion1nstd206human GRCh38 chr3: 146,074,387-146,074,438 , GRCh37.p13 chr3: 145,792,174-145,792,225 PLOD2
    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
    nsv5367082translocation1nstd200human GRCh38 chr3: 146,126,913-146,126,913 , GRCh38 chr3: 146,126,606-146,126,606 , GRCh37.p13 chr3: 145,844,700-145,844,700 , GRCh37.p13 chr3: 145,844,393-145,844,393 PLOD2
    nsv5301803copy number variation1nstd204human GRCh38.p13 chr3: 145,088,231-147,513,312 , GRCh37.p13 chr3: 144,806,005-147,231,099 LINC02010, ZIC1, 21 more genes
    nsv5232502copy number variation1nstd204human GRCh38.p13 chr3: 145,088,201-146,733,600 , GRCh37.p13 chr3: 144,805,975-146,451,387 PLSCR2, LOC105374143, 14 more genes
    nsv5230776copy number variation1nstd204human GRCh38.p13 chr3: 146,087,501-146,093,600 , GRCh37.p13 chr3: 145,805,288-145,811,387 PLOD2
    nsv5222289copy number variation1nstd204human GRCh38.p13 chr3: 146,161,489-146,163,188 , GRCh37.p13 chr3: 145,879,276-145,880,975 PLOD2, LOC105374145
    nsv5182086mobile element insertion1nstd203human GRCh38 chr3: 146,144,168-146,144,185 , GRCh37.p13 chr3: 145,861,955-145,861,972 PLOD2
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv5034922inversion1nstd200human GRCh38 chr3: 137,979,992-148,451,901 , GRCh37.p13 chr3: 137,698,834-148,169,688 , LOC105374148, 132 more genes
    nsv4914865copy number variation1nstd200human GRCh38 chr3: 145,886,271-146,782,511 , GRCh37.p13 chr3: 145,604,058-146,500,298 LOC105374145, PLSCR4P1, 8 more genes
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