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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142279insertion1nstd232human GRCh37.p13 chr19: 15,761,622-15,761,622 , GRCh38.p12 chr19: 15,650,812-15,650,812 CYP4F3
    nsv7098925copy number variation1nstd102humanPathogenic GRCh38 chr19: 15,014,099-16,261,691 , GRCh37.p13 chr19: 15,124,911-16,372,502 CYP4F12, OR1AB1P, 52 more genes
    nsv7095645copy number variation1nstd102humanUncertain significance GRCh37 chr19: 14,847,048-17,394,124 , GRCh38.p12 chr19: 14,736,236-17,283,315 HAUS8, MIR1470, 95 more genes
    nsv7075473inversion1nstd229human GRCh38 chr19: 12,694,752-17,614,167 , GRCh37.p13 chr19: 12,805,566-17,724,976 SYDE1, LOC107985287, 207 more genes
    nsv7065580inversion1nstd229human GRCh38 chr19: 11,963,576-20,150,892 , GRCh37.p13 chr19: 12,074,391-20,193,556 CYP4F24P, CYP4F2, 359 more genes
    nsv7064525inversion1nstd229human GRCh38 chr19: 15,479,233-16,002,161 , GRCh37.p13 chr19: 15,590,044-16,112,971 CLEC4OP, LOC100422106, 24 more genes
    nsv7063135inversion1nstd229human GRCh38 chr19: 12,625,698-17,530,884 , GRCh37.p13 chr19: 12,736,512-17,641,693 SYCE2, OR1AB1P, 212 more genes
    nsv7060542inversion1nstd229human GRCh38 chr19: 12,342,956-19,691,233 , GRCh37.p13 chr19: 12,453,770-19,802,042 DDX39A, KCNN1, 314 more genes
    nsv7059139inversion1nstd229human GRCh38 chr19: 12,641,624-19,910,103 , GRCh37.p13 chr19: 12,752,438-20,020,912 NR2F6, ISCA1P5, 307 more genes
    nsv7011468copy number variation1nstd229human GRCh38 chr19: 15,655,701-15,669,300 , GRCh37.p13 chr19: 15,766,511-15,780,110 CYP4F3, CYP4F10P
    nsv7008978copy number variation1nstd229human GRCh38 chr19: 15,655,395-15,703,173 , GRCh37.p13 chr19: 15,766,205-15,813,983 CYP4F3, CYP4F10P, 1 more genes
    nsv7003828copy number variation1nstd229human GRCh38 chr19: 15,654,672-15,801,391 , GRCh37.p13 chr19: 15,765,482-15,912,201 OR10H5, OR10H3, 5 more genes
    nsv7002756copy number variation1nstd229human GRCh38 chr19: 15,651,164-15,651,599 , GRCh37.p13 chr19: 15,761,974-15,762,409 CYP4F3
    nsv7000581copy number variation1nstd229human GRCh38 chr19: 15,643,214-15,643,306 , GRCh37.p13 chr19: 15,754,024-15,754,116 CYP4F3
    nsv7000098copy number variation1nstd229human GRCh38 chr19: 15,639,781-15,639,818 , GRCh37.p13 chr19: 15,750,591-15,750,628 CYP4F3
    nsv6998373copy number variation1nstd229human GRCh38 chr19: 15,633,385-15,641,680 , GRCh37.p13 chr19: 15,744,195-15,752,490 CYP4F3
    nsv6624833copy number variation1nstd224human GRCh37 chr19: 15,760,015-15,772,414 , GRCh38.p12 chr19: 15,649,205-15,661,604 CYP4F3
    nsv6599077inversion1nstd223human GRCh38 chr19: 12,342,953-19,691,233 , GRCh37.p13 chr19: 12,453,767-19,802,042 GET3, BST2, 314 more genes
    nsv6527434copy number variation1nstd223human GRCh38 chr19: 15,647,304-15,664,381 , GRCh37.p13 chr19: 15,758,114-15,775,191 CYP4F10P, CYP4F3
    nsv6526542copy number variation1nstd223human GRCh38 chr19: 15,651,223-15,651,891 , GRCh37.p13 chr19: 15,762,033-15,762,701 CYP4F3
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