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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv5979349insertion1nstd209human GRCh38 chr18: 47,882,041-47,882,041 , GRCh37.p13 chr18: 45,408,412-45,408,412 SMAD2
    nsv5942802copy number variation1nstd209human GRCh38 chr18: 47,850,374-47,850,685 , GRCh37.p13 chr18: 45,376,745-45,377,056 SMAD2
    nsv5936476copy number variation1nstd209human GRCh38 chr18: 47,850,624-47,850,848 , GRCh37.p13 chr18: 45,376,995-45,377,219 SMAD2
    nsv5934873copy number variation1nstd209human GRCh38 chr18: 47,853,242-47,853,435 , GRCh37.p13 chr18: 45,379,613-45,379,806 MTCO2P2, SMAD2
    nsv5929384copy number variation1nstd209human GRCh38 chr18: 47,850,361-47,850,543 , GRCh37.p13 chr18: 45,376,732-45,376,914 SMAD2
    nsv5928789copy number variation1nstd209human GRCh38 chr18: 47,828,221-47,828,304 , GRCh37.p13 chr18: 45,354,592-45,354,675 SMAD2
    nsv5880034copy number variation1nstd209human GRCh38 chr18: 47,923,877-47,926,276 , GRCh37.p13 chr18: 45,450,248-45,452,647 SMAD2
    nsv5704884mobile element insertion1nstd211human GRCh38 chr18: 47,856,728-47,856,728 , GRCh37.p13 chr18: 45,383,099-45,383,099 SMAD2
    nsv5662770insertion1nstd207human GRCh38 chr18: 47,882,041-47,882,041 , GRCh37.p13 chr18: 45,408,412-45,408,412 SMAD2
    nsv5658853insertion1nstd207human GRCh38 chr18: 47,850,803-47,850,803 , GRCh37.p13 chr18: 45,377,174-45,377,174 SMAD2
    nsv5656280insertion2nstd207human GRCh38 chr18: 47,850,396-47,850,396 , GRCh37.p13 chr18: 45,376,767-45,376,767 SMAD2
    nsv5654055insertion1nstd207human GRCh38 chr18: 47,850,481-47,850,481 , GRCh37.p13 chr18: 45,376,852-45,376,852 SMAD2
    nsv5646099insertion1nstd207human GRCh38 chr18: 47,850,232-47,850,232 , GRCh37.p13 chr18: 45,376,603-45,376,603 SMAD2
    nsv5602401copy number variation1nstd207human GRCh38 chr18: 47,850,301-47,850,505 , GRCh37.p13 chr18: 45,376,672-45,376,876 SMAD2
    nsv5597533copy number variation1nstd207human GRCh38 chr18: 47,850,667-47,850,786 , GRCh37.p13 chr18: 45,377,038-45,377,157 SMAD2
    nsv5592608copy number variation1nstd207human GRCh38 chr18: 47,850,710-47,850,786 , GRCh37.p13 chr18: 45,377,081-45,377,157 SMAD2
    nsv5591983copy number variation1nstd207human GRCh38 chr18: 47,853,242-47,853,435 , GRCh37.p13 chr18: 45,379,613-45,379,806 MTCO2P2, SMAD2
    nsv5533409copy number variation1nstd206human GRCh38 chr18: 47,886,595-47,886,780 , GRCh37.p13 chr18: 45,412,966-45,413,151 SMAD2
    nsv5532994copy number variation1nstd206human GRCh38 chr18: 47,841,096-47,841,577 , GRCh37.p13 chr18: 45,367,467-45,367,948 SMAD2
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