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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 more genes
    nsv5528381copy number variation1nstd206human GRCh38 chr19: 13,002,506-13,002,572 , GRCh37.p13 chr19: 13,113,320-13,113,386 NFIX
    nsv5515853copy number variation1nstd206human GRCh38 chr19: 13,010,099-13,010,226 , GRCh37.p13 chr19: 13,120,913-13,121,040 NFIX
    nsv5381052copy number variation1nstd102humanUncertain significance GRCh37 chr19: 13,135,448-13,574,132 , GRCh38.p12 chr19: 13,024,634-13,463,318 IER2, CACNA1A, 7 more genes
    nsv5332790translocation1nstd200human GRCh37 chr19: 13,161,430-13,161,430 , GRCh37 chr19: 13,161,324-13,161,324 , GRCh38.p12 chr19: 13,050,510-13,050,510 , GRCh38.p12 chr19: 13,050,616-13,050,616 NFIX
    nsv5282549copy number variation1nstd204human GRCh38.p13 chr19: 12,584,101-13,543,500 , GRCh37.p13 chr19: 12,694,915-13,654,314 , NFIX, 50 more genes
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv5014550copy number variation1nstd200human GRCh38 chr19: 13,037,030-13,037,502 , GRCh37.p13 chr19: 13,147,844-13,148,316 NFIX
    nsv5011840copy number variation1nstd200human GRCh38 chr19: 13,083,517-13,083,668 , GRCh37.p13 chr19: 13,194,331-13,194,482 NFIX
    nsv5011839copy number variation1nstd200human GRCh38 chr19: 13,050,510-13,050,616 , GRCh37.p13 chr19: 13,161,324-13,161,430 NFIX
    nsv5011838copy number variation1nstd200human GRCh38 chr19: 13,010,098-13,010,226 , GRCh37.p13 chr19: 13,120,912-13,121,040 NFIX
    nsv4864941copy number variation1nstd200human GRCh37 chr19: 13,147,844-13,148,316 , GRCh38.p12 chr19: 13,037,030-13,037,502 NFIX
    nsv4860360copy number variation1nstd200human GRCh37 chr19: 13,195,024-13,195,605 , GRCh38.p12 chr19: 13,084,210-13,084,791 NFIX
    nsv4860359copy number variation1nstd200human GRCh37 chr19: 13,120,913-13,121,040 , GRCh38.p12 chr19: 13,010,099-13,010,226 NFIX
    nsv4769313copy number variation1nstd102humanPathogenic GRCh37 chr19: 13,185,842-13,191,771 , GRCh38 chr19: 13,075,028-13,080,957 NFIX
    nsv4683040copy number variation1nstd102humanPathogenic GRCh37 chr19: 13,198,783-13,205,483 , GRCh38.p12 chr19: 13,087,969-13,094,669 NFIX
    nsv4681475copy number variation1nstd102humanPathogenic GRCh37 chr19: 13,185,396-13,188,618 , GRCh38 chr19: 13,074,582-13,077,804 NFIX
    nsv4669601copy number variation1nstd186human GRCh37 chr19: 13,101,920-13,106,684 , GRCh38.p12 chr19: 12,991,106-12,995,870 NFIX
    nsv4622601copy number variation1nstd183human GRCh37 chr19: 13,101,920-13,106,684 , GRCh38.p12 chr19: 12,991,106-12,995,870 NFIX
    nsv4578606copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 13,135,810-13,136,366 , GRCh38.p12 chr19: 13,024,996-13,025,552 NFIX
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