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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112761copy number variation1nstd102humanPathogenic GRCh37 chr4: 69,671-29,702,595 , GRCh38.p12 chr4: 69,779-29,700,973 LOC101928306, PDE6B-AS1, 460 more genes
    nsv6112747copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,598-18,912,995 , GRCh38.p12 chr4: 68,706-18,911,372 GPR78, LOC105374510, 362 more genes
    nsv5955427insertion1nstd209human GRCh38 chr4: 17,721,383-17,721,383 , GRCh37.p13 chr4: 17,723,006-17,723,006 FAM184B
    nsv5954565insertion1nstd209human GRCh38 chr4: 17,653,919-17,653,919 , GRCh37.p13 chr4: 17,655,542-17,655,542 FAM184B
    nsv5683559mobile element insertion1nstd211human GRCh38 chr4: 17,731,552-17,731,552 , GRCh37.p13 chr4: 17,733,175-17,733,175 FAM184B
    nsv5680105mobile element insertion2nstd211human GRCh38 chr4: 17,757,737-17,757,737 , GRCh37.p13 chr4: 17,759,360-17,759,360 FAM184B
    nsv5677439mobile element insertion1nstd211human GRCh38 chr4: 17,768,241-17,768,241 , GRCh37.p13 chr4: 17,769,864-17,769,864 FAM184B
    nsv5622994insertion1nstd207human GRCh38 chr4: 17,735,643-17,735,643 , GRCh37.p13 chr4: 17,737,266-17,737,266 FAM184B
    nsv5618417insertion1nstd207human GRCh38 chr4: 17,757,727-17,757,727 , GRCh37.p13 chr4: 17,759,350-17,759,350 FAM184B
    nsv5613645insertion1nstd207human GRCh38 chr4: 17,764,813-17,764,813 , GRCh37.p13 chr4: 17,766,436-17,766,436 FAM184B
    nsv5611921insertion1nstd207human GRCh38 chr4: 17,653,919-17,653,919 , GRCh37.p13 chr4: 17,655,542-17,655,542 FAM184B
    nsv5606185insertion1nstd207human GRCh38 chr4: 17,717,107-17,717,107 , GRCh37.p13 chr4: 17,718,730-17,718,730 FAM184B
    nsv5552817insertion1nstd206human GRCh38 chr4: 17,717,125-17,717,158 , GRCh37.p13 chr4: 17,718,748-17,718,781 FAM184B
    nsv5552711insertion1nstd206human GRCh38 chr4: 17,653,926-17,653,938 , GRCh37.p13 chr4: 17,655,549-17,655,561 FAM184B
    nsv5552553insertion1nstd206human GRCh38 chr4: 17,735,643-17,735,643 , GRCh37.p13 chr4: 17,737,266-17,737,266 FAM184B
    nsv5542853insertion1nstd206human GRCh38 chr4: 17,764,813-17,764,813 , GRCh37.p13 chr4: 17,766,436-17,766,436 FAM184B
    nsv5441848copy number variation1nstd206human GRCh38 chr4: 17,710,017-17,714,800 , GRCh37.p13 chr4: 17,711,640-17,716,423 FAM184B
    nsv5439880copy number variation1nstd206human GRCh38 chr4: 17,714,457-17,714,646 , GRCh37.p13 chr4: 17,716,080-17,716,269 FAM184B
    nsv5434972copy number variation1nstd206human GRCh38 chr4: 17,720,796-17,737,149 , GRCh37.p13 chr4: 17,722,419-17,738,772 FAM184B
    nsv5406954mobile element insertion1nstd206human GRCh38 chr4: 17,768,241-17,768,292 , GRCh37.p13 chr4: 17,769,864-17,769,915 FAM184B
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