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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
    nsv5707808mobile element insertion2nstd211human GRCh38 chr18: 32,189,482-32,189,482 , GRCh37.p13 chr18: 29,769,445-29,769,445 MEP1B
    nsv5419774mobile element insertion1nstd206human GRCh38 chr18: 32,189,482-32,189,533 , GRCh37.p13 chr18: 29,769,445-29,769,496 MEP1B
    nsv5321444copy number variation1nstd204human GRCh37.p13 chr18: 29,731,981-29,810,913 , GRCh38.p13 chr18: 32,152,018-32,230,950 MEP1B, CLUHP6, 1 more genes
    nsv5297881copy number variation1nstd204human GRCh38.p13 chr18: 32,218,714-32,219,978 , GRCh37.p13 chr18: 29,798,677-29,799,941 MEP1B
    nsv5291542copy number variation1nstd204human GRCh38.p13 chr18: 32,219,314-32,220,378 , GRCh37.p13 chr18: 29,799,277-29,800,341 MEP1B
    nsv5289333copy number variation1nstd204human GRCh38.p13 chr18: 32,152,401-32,230,900 , GRCh37.p13 chr18: 29,732,364-29,810,863 RNA5SP453, MEP1B, 1 more genes
    nsv5289233copy number variation1nstd204human GRCh38.p13 chr18: 32,208,902-32,210,040 , GRCh37.p13 chr18: 29,788,865-29,790,003 MEP1B
    nsv5287981copy number variation1nstd204human GRCh38.p13 chr18: 32,190,075-32,197,224 , GRCh37.p13 chr18: 29,770,038-29,777,187 CLUHP6, MEP1B
    nsv5287891copy number variation1nstd204human GRCh38.p13 chr18: 32,197,725-32,228,018 , GRCh37.p13 chr18: 29,777,688-29,807,981 MEP1B
    nsv5287742copy number variation1nstd204human GRCh38.p13 chr18: 32,189,375-32,190,674 , GRCh37.p13 chr18: 29,769,338-29,770,637 MEP1B
    nsv5287550copy number variation1nstd204human GRCh38.p13 chr18: 32,203,902-32,204,901 , GRCh37.p13 chr18: 29,783,865-29,784,864 MEP1B
    nsv5283952copy number variation1nstd204human GRCh38.p13 chr18: 32,207,902-32,208,901 , GRCh37.p13 chr18: 29,787,865-29,788,864 MEP1B
    nsv5282232copy number variation1nstd204human GRCh38.p13 chr18: 32,193,301-32,231,000 , GRCh37.p13 chr18: 29,773,264-29,810,963 MEP1B, CLUHP6
    nsv5155382mobile element insertion1nstd203human GRCh38 chr18: 32,189,466-32,189,482 , GRCh37.p13 chr18: 29,769,429-29,769,445 MEP1B
    nsv5024081copy number variation1nstd200human GRCh38 chr18: 32,206,933-32,263,391 , GRCh37.p13 chr18: 29,786,896-29,843,354 GAREM1, MEP1B
    nsv5011204copy number variation1nstd200human GRCh38 chr18: 32,152,017-32,230,940 , GRCh37.p13 chr18: 29,731,980-29,810,903 MEP1B, RNA5SP453, 1 more genes
    nsv4859166copy number variation1nstd200human GRCh37 chr18: 29,731,972-29,810,914 , GRCh38.p12 chr18: 32,152,009-32,230,951 MEP1B, RNA5SP453, 1 more genes
    nsv4854629copy number variation1nstd200human GRCh37 chr18: 29,786,896-29,843,354 , GRCh38.p12 chr18: 32,206,933-32,263,391 MEP1B, GAREM1
    nsv4729854copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,971,647-33,737,300 , GRCh38.p12 chr18: 26,391,683-36,157,337 CLUHP6, KLHL14, 100 more genes
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