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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5948908insertion1nstd209human GRCh38 chr2: 120,163,969-120,163,969 , GRCh37.p13 chr2: 120,921,545-120,921,545 EPB41L5, LOC105373582
    nsv5901384copy number variation1nstd209human GRCh38 chr2: 120,016,693-120,016,866 , GRCh37.p13 chr2: 120,774,269-120,774,442 EPB41L5
    nsv5728597mobile element insertion1nstd211human GRCh38 chr2: 120,092,869-120,092,869 , GRCh37.p13 chr2: 120,850,445-120,850,445 EPB41L5
    nsv5725343mobile element insertion1nstd211human GRCh38 chr2: 120,045,271-120,045,271 , GRCh37.p13 chr2: 120,802,847-120,802,847 EPB41L5
    nsv5692028mobile element insertion2nstd211human GRCh38 chr2: 120,149,179-120,149,179 , GRCh37.p13 chr2: 120,906,755-120,906,755 EPB41L5
    nsv5689459mobile element insertion2nstd211human GRCh38 chr2: 120,096,133-120,096,133 , GRCh37.p13 chr2: 120,853,709-120,853,709 EPB41L5
    nsv5681318mobile element insertion1nstd211human GRCh38 chr2: 120,099,363-120,099,363 , GRCh37.p13 chr2: 120,856,939-120,856,939 EPB41L5
    nsv5563099mobile element insertion1nstd206human GRCh38 chr2: 120,045,271-120,045,322 , GRCh37.p13 chr2: 120,802,847-120,802,898 EPB41L5
    nsv5558142mobile element insertion1nstd206human GRCh38 chr2: 102,295,972-141,288,199 , GRCh37.p13 chr2: 102,912,432-142,045,768 , LOC105373587, 623 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5544680insertion1nstd206human GRCh38 chr2: 120,149,179-120,149,213 , GRCh37.p13 chr2: 120,906,755-120,906,789 EPB41L5
    nsv5450742copy number variation1nstd206human GRCh38 chr2: 120,016,695-120,016,867 , GRCh37.p13 chr2: 120,774,271-120,774,443 EPB41L5
    nsv5441281copy number variation1nstd206human GRCh38 chr2: 120,101,720-120,101,808 , GRCh37.p13 chr2: 120,859,296-120,859,384 EPB41L5
    nsv5440524copy number variation1nstd206human GRCh38 chr2: 120,169,149-120,169,215 , GRCh37.p13 chr2: 120,926,725-120,926,791 LOC105373582, EPB41L5
    nsv5438563copy number variation1nstd206human GRCh38 chr2: 120,160,300-120,160,439 , GRCh37.p13 chr2: 120,917,876-120,918,015 EPB41L5
    nsv5405986mobile element insertion1nstd206human GRCh38 chr2: 120,096,133-120,096,184 , GRCh37.p13 chr2: 120,853,709-120,853,760 EPB41L5
    nsv5361072translocation1nstd200human GRCh38 chr2: 120,179,142-120,179,142 , GRCh38 chr2: 120,179,195-120,179,195 , GRCh37.p13 chr2: 120,936,771-120,936,771 , GRCh37.p13 chr2: 120,936,718-120,936,718 EPB41L5
    nsv5339473translocation1nstd200human GRCh37 chr2: 120,774,443-120,774,443 , GRCh37 chr2: 120,774,271-120,774,271 , GRCh38.p12 chr2: 120,016,867-120,016,867 , GRCh38.p12 chr2: 120,016,695-120,016,695 EPB41L5
    nsv5298699copy number variation1nstd204human GRCh38.p13 chr2: 120,117,785-120,121,071 , GRCh37.p13 chr2: 120,875,361-120,878,647 EPB41L5
    nsv5285964copy number variation1nstd204human GRCh37.p13 chr2: 120,737,869-120,794,546 , GRCh38.p13 chr2: 119,980,293-120,036,970 PTPN4, EPB41L5, 2 more genes
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