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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095205copy number variation2nstd102humanUncertain significance GRCh37 chr19: 39,205,089-40,913,839 , GRCh38.p12 chr19: 38,714,449-40,407,932 CCNP, NFKBIB, 81 more genes
    nsv7075514inversion1nstd229human GRCh38 chr19: 38,994,526-39,502,034 , GRCh37.p13 chr19: 39,485,166-39,992,674 RPS16, PLEKHG2, 25 more genes
    nsv7071361inversion1nstd229human GRCh38 chr19: 39,004,066-42,402,005 , GRCh37.p13 chr19: 39,494,706-42,906,157 RAB4B, RABAC1, 160 more genes
    nsv7068288inversion1nstd229human GRCh38 chr19: 39,023,970-42,945,419 , GRCh37.p13 chr19: 39,514,610-43,449,571 MIR4530, RNU6-195P, 178 more genes
    nsv7010804copy number variation1nstd229human GRCh38 chr19: 39,236,049-39,293,000 , GRCh37.p13 chr19: 39,726,689-39,783,640 IFNL3, IFNL4P1, 4 more genes
    nsv7008156copy number variation1nstd229human GRCh38 chr19: 36,851,242-46,031,790 , GRCh37.p13 chr19: 37,342,144-46,535,048 LOC105372390, LOC107985291, 396 more genes
    nsv7005713copy number variation1nstd229human GRCh38 chr19: 33,458,650-39,721,746 , GRCh37.p13 chr19: 33,949,556-40,212,386 , TYROBP, 259 more genes
    nsv7002869copy number variation1nstd229human GRCh38 chr19: 38,872,385-39,331,882 , GRCh37.p13 chr19: 39,363,025-39,822,522 IFNL4P1, IFNL4, 19 more genes
    nsv6531882copy number variation1nstd223human GRCh38 chr19: 38,872,385-39,331,882 , GRCh37.p13 chr19: 39,363,025-39,822,522 NFKBIB, IFNL3, 19 more genes
    nsv6517909copy number variation1nstd223human GRCh38 chr19: 39,264,144-39,272,790 , GRCh37.p13 chr19: 39,754,784-39,763,430 IFNL4P1, IFNL2
    nsv6290300copy number variation1nstd102humanPathogenic GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324 ZNF420, LOC105372330, 574 more genes
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv5656506insertion1nstd207human GRCh38 chr19: 39,267,335-39,267,335 , GRCh37.p13 chr19: 39,757,975-39,757,975 IFNL2
    nsv5027938copy number variation1nstd200human GRCh38 chr19: 39,264,144-39,272,793 , GRCh37.p13 chr19: 39,754,784-39,763,433 IFNL2, IFNL4P1
    nsv5024626copy number variation1nstd200human GRCh38 chr19: 39,188,419-39,288,169 , GRCh37.p13 chr19: 39,679,059-39,778,809 IFNL3, SYCN, 6 more genes
    nsv4865165copy number variation1nstd200human GRCh37 chr19: 39,679,059-39,778,809 , GRCh38.p12 chr19: 39,188,419-39,288,169 IFNL2, NCCRP1, 6 more genes
    nsv4620623copy number variation1nstd183human GRCh37 chr19: 39,759,311-39,759,355 , GRCh38.p12 chr19: 39,268,671-39,268,715 IFNL2
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4270000copy number variation1nstd166human GRCh37.p13 chr19: 39,679,116-39,778,738 , GRCh38.p12 chr19: 39,188,476-39,288,098 IFNL2, IFNL3, 6 more genes
    nsv3928333insertion1nstd167human GRCh37 chr19: 39,758,623-39,758,623 , GRCh38.p12 chr19: 39,267,983-39,267,983 IFNL2
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