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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6128531copy number variation1nstd186human GRCh37 chr19: 1,209,380-1,216,434 , GRCh38.p12 chr19: 1,209,381-1,216,435 STK11
    nsv5942044copy number variation1nstd209human GRCh38 chr19: 1,208,418-1,208,727 , GRCh37.p13 chr19: 1,208,417-1,208,726 STK11
    nsv5934300copy number variation1nstd209human GRCh38 chr19: 1,208,175-1,208,231 , GRCh37.p13 chr19: 1,208,174-1,208,230 STK11
    nsv5673387copy number variation1nstd102humanPathogenic GRCh37 chr19: 1,221,107-1,227,749 , GRCh38.p12 chr19: 1,221,108-1,227,750 CBARP, STK11
    nsv5673386copy number variation1nstd102humanPathogenic GRCh37 chr19: 1,220,366-1,220,510 , GRCh38.p12 chr19: 1,220,367-1,220,511 STK11
    nsv5673385copy number variation1nstd102humanPathogenic GRCh37 chr19: 1,218,406-1,218,509 , GRCh38.p12 chr19: 1,218,407-1,218,510 STK11
    nsv5673229copy number variation1nstd102humanPathogenic GRCh37 chr19: 1,206,903-1,207,212 , GRCh38.p12 chr19: 1,206,904-1,207,213 STK11
    nsv5673069copy number variation1nstd102humanPathogenic GRCh37 chr19: 1,206,907-1,226,652 , GRCh38.p12 chr19: 1,206,908-1,226,653 STK11, CBARP
    nsv5672905copy number variation1nstd102humanPathogenic GRCh37 chr19: 1,218,406-1,219,422 , GRCh38.p12 chr19: 1,218,407-1,219,423 STK11
    nsv5592670copy number variation1nstd207human GRCh38 chr19: 1,208,175-1,208,231 , GRCh37.p13 chr19: 1,208,174-1,208,230 STK11
    nsv5564316copy number variation1nstd102humanPathogenic GRCh37 chr19: 1,206,911-1,208,215 , GRCh38 chr19: 1,206,912-1,208,216 STK11
    nsv5564231copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 1,218,413-1,218,589 , GRCh38 chr19: 1,218,414-1,218,590 STK11
    nsv5530338copy number variation1nstd206human GRCh38 chr19: 1,209,381-1,216,435 , GRCh37.p13 chr19: 1,209,380-1,216,434 STK11
    nsv5514112copy number variation1nstd206human GRCh38 chr19: 1,208,176-1,208,232 , GRCh37.p13 chr19: 1,208,175-1,208,231 STK11
    nsv5381051copy number variation1nstd102humanUncertain significance GRCh37 chr19: 1,206,913-1,222,015 , GRCh38.p12 chr19: 1,206,914-1,222,016 STK11
    nsv5328740copy number variation1nstd204human GRCh38.p13 chr19: 928,886-1,307,166 , GRCh37.p13 chr19: 928,886-1,307,165 RNU6-2, CNN2, 25 more genes
    nsv5299463copy number variation1nstd204human GRCh38.p13 chr19: 1,203,316-1,205,499 , GRCh37.p13 chr19: 1,203,315-1,205,498 HMGB2P1, STK11
    nsv5293566copy number variation1nstd204human GRCh38.p13 chr19: 1,197,501-1,413,600 , GRCh37.p13 chr19: 1,197,500-1,413,599 CBARP, RPS15P9, 17 more genes
    nsv5293535copy number variation1nstd204human GRCh38.p13 chr19: 1,208,424-1,209,967 , GRCh37.p13 chr19: 1,208,423-1,209,966 STK11
    nsv5292395copy number variation1nstd204human GRCh38.p13 chr19: 1,215,675-1,218,174 , GRCh37.p13 chr19: 1,215,674-1,218,173 STK11
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