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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5512947copy number variation1nstd206human GRCh38 chr13: 37,584,535-37,584,605 , GRCh37.p13 chr13: 38,158,672-38,158,742 POSTN
    nsv5507908copy number variation1nstd206human GRCh38 chr13: 37,576,736-37,576,814 , GRCh37.p13 chr13: 38,150,873-38,150,951 POSTN
    nsv5274439copy number variation1nstd204human GRCh38.p13 chr13: 37,569,301-37,573,200 , GRCh37.p13 chr13: 38,143,438-38,147,337 POSTN
    nsv5264425copy number variation1nstd204human GRCh38.p13 chr13: 37,560,801-37,575,300 , GRCh37.p13 chr13: 38,134,938-38,149,437 POSTN
    nsv5155419mobile element insertion1nstd203human GRCh38 chr13: 37,567,187-37,567,235 , GRCh37.p13 chr13: 38,141,324-38,141,372 POSTN
    nsv5155103mobile element insertion1nstd203human GRCh38 chr13: 37,567,204-37,567,235 , GRCh37.p13 chr13: 38,141,341-38,141,372 POSTN
    nsv5151207mobile element insertion1nstd203human GRCh38 chr13: 37,567,226-37,567,235 , GRCh37.p13 chr13: 38,141,363-38,141,372 POSTN
    nsv5148908mobile element insertion1nstd203human GRCh38 chr13: 37,567,201-37,567,235 , GRCh37.p13 chr13: 38,141,338-38,141,372 POSTN
    nsv5144535mobile element insertion1nstd203human GRCh38 chr13: 37,567,200-37,567,235 , GRCh37.p13 chr13: 38,141,337-38,141,372 POSTN
    nsv5004456copy number variation1nstd200human GRCh38 chr13: 31,196,586-38,438,583 , GRCh37.p13 chr13: 31,770,723-39,012,720 , LOC102723490, 82 more genes
    nsv4997027copy number variation1nstd200human GRCh38 chr13: 37,567,401-37,568,711 , GRCh37.p13 chr13: 38,141,538-38,142,848 POSTN
    nsv4997012copy number variation1nstd200human GRCh38 chr13: 37,242,817-37,628,733 , GRCh37.p13 chr13: 37,816,954-38,202,870 LINC00547, LINC01048, 1 more genes
    nsv4835509copy number variation1nstd200human GRCh37 chr13: 38,143,950-38,149,123 , GRCh38.p12 chr13: 37,569,813-37,574,986 POSTN
    nsv4833225copy number variation1nstd200human GRCh37 chr13: 38,135,720-38,136,018 , GRCh38.p12 chr13: 37,561,583-37,561,881 POSTN
    nsv4675966copy number variation1nstd102humanLikely benign GRCh37 chr13: 37,730,506-38,751,741 , GRCh38.p12 chr13: 37,156,369-38,177,604 LINC01048, LINC02334, 9 more genes
    nsv4530093copy number variation1nstd166human GRCh37.p13 chr13: 38,137,696-38,138,346 , GRCh38.p12 chr13: 37,563,559-37,564,209 POSTN
    nsv4510899mobile element insertion1nstd166human GRCh37.p13 chr13: 38,153,632-38,153,632 , GRCh38.p12 chr13: 37,579,495-37,579,495 POSTN
    nsv4230977copy number variation1nstd166human GRCh37.p13 chr13: 38,015,796-38,167,772 , GRCh38.p12 chr13: 37,441,659-37,593,635 LINC00547, LINC01048, 1 more genes
    nsv4227784copy number variation1nstd166human GRCh37.p13 chr13: 38,150,872-38,150,951 , GRCh38.p12 chr13: 37,576,735-37,576,814 POSTN
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