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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137808copy number variation1nstd102humanLikely pathogenic GRCh38.p12 chr19: 49,568,107-49,662,685 , GRCh37 chr19: 50,071,364-50,165,942 IRF3, PRRG2, 4 more genes
    nsv6128806copy number variation1nstd186human GRCh37 chr19: 50,114,898-50,115,191 , GRCh38.p12 chr19: 49,611,641-49,611,934 PRR12
    nsv5940616copy number variation1nstd209human GRCh38 chr19: 49,611,641-49,611,930 , GRCh37.p13 chr19: 50,114,898-50,115,187 PRR12
    nsv5931299copy number variation1nstd209human GRCh38 chr19: 49,604,921-49,605,331 , GRCh37.p13 chr19: 50,108,178-50,108,588 PRR12
    nsv5667352inversion1nstd207human GRCh38 chr19: 47,959,661-50,091,195 , GRCh37.p13 chr19: 48,462,918-50,594,452 , AP2A1, 145 more genes
    nsv5649952insertion1nstd207human GRCh38 chr19: 49,624,317-49,624,317 , GRCh37.p13 chr19: 50,127,574-50,127,574 PRR12
    nsv5647808insertion1nstd207human GRCh38 chr19: 49,623,799-49,623,799 , GRCh37.p13 chr19: 50,127,056-50,127,056 PRR12
    nsv5592224copy number variation1nstd207human GRCh38 chr19: 49,623,799-49,623,864 , GRCh37.p13 chr19: 50,127,056-50,127,121 PRR12
    nsv5588303copy number variation1nstd207human GRCh38 chr19: 49,621,134-49,621,184 , GRCh37.p13 chr19: 50,124,391-50,124,441 PRR12
    nsv5526836copy number variation1nstd206human GRCh38 chr19: 49,624,247-49,624,328 , GRCh37.p13 chr19: 50,127,504-50,127,585 PRR12
    nsv5518521copy number variation1nstd206human GRCh38 chr19: 49,611,641-49,611,934 , GRCh37.p13 chr19: 50,114,898-50,115,191 PRR12
    nsv5385246mobile element deletion1nstd186human GRCh37 chr19: 50,114,898-50,115,179 , GRCh38.p12 chr19: 49,611,641-49,611,922 PRR12
    nsv5382459mobile element deletion1nstd186human GRCh37 chr19: 50,114,897-50,115,179 , GRCh38.p12 chr19: 49,611,640-49,611,922 PRR12
    nsv5359886translocation1nstd200human GRCh38 chr19: 49,608,888-49,608,888 , GRCh38 chr19: 49,608,960-49,608,960 , GRCh37.p13 chr19: 50,112,145-50,112,145 , GRCh37.p13 chr19: 50,112,217-50,112,217 PRR12
    nsv5328199copy number variation1nstd204human GRCh38.p13 chr19: 49,623,915-49,624,471 , GRCh37.p13 chr19: 50,127,172-50,127,728 PRR12
    nsv5322541copy number variation1nstd204human GRCh38.p13 chr19: 49,611,600-49,612,029 , GRCh37.p13 chr19: 50,114,857-50,115,286 PRR12
    nsv5172611mobile element insertion1nstd203human GRCh38 chr19: 49,607,424-49,607,424 , GRCh37.p13 chr19: 50,110,681-50,110,681 PRR12
    nsv5024814copy number variation1nstd200human GRCh38 chr19: 49,603,846-49,610,166 , GRCh37.p13 chr19: 50,107,103-50,113,423 PRR12
    nsv4907561mobile element deletion1nstd200human GRCh38 chr19: 49,611,638-49,611,924 , GRCh37.p13 chr19: 50,114,895-50,115,181 PRR12
    nsv4853338copy number variation1nstd200human GRCh37 chr19: 50,127,180-50,127,720 , GRCh38.p12 chr19: 49,623,923-49,624,463 PRR12
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