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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095639copy number variation2nstd102humanUncertain significance GRCh37 chr19: 13,135,448-13,419,362 , GRCh38.p12 chr19: 13,024,634-13,308,548 IER2, RPL12P42, 7 more genes
    nsv7095458copy number variation4nstd102humanUncertain significance GRCh37 chr19: 10,828,919-13,482,613 , GRCh38.p12 chr19: 10,718,243-13,371,799 WDR83OS, RPL10P16, 140 more genes
    nsv7095400copy number variation1nstd102humanUncertain significance GRCh37 chr19: 11,277,234-13,249,220 , GRCh38.p12 chr19: 11,166,558-13,138,406 ZNF627, RGL3, 120 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
    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
    nsv6599077inversion1nstd223human GRCh38 chr19: 12,342,953-19,691,233 , GRCh37.p13 chr19: 12,453,767-19,802,042 GET3, BST2, 314 more genes
    nsv6524850copy number variation1nstd223human GRCh38 chr19: 13,102,002-13,103,524 , GRCh37.p13 chr19: 13,212,816-13,214,338 LYL1, LOC105372282, 1 more genes
    nsv6523555copy number variation1nstd223human GRCh38 chr19: 13,096,601-13,097,300 , GRCh37.p13 chr19: 13,207,415-13,208,114 NFIX, LYL1
    nsv6310462copy number variation2nstd102humanPathogenic GRCh37 chr19: 12,757,434-13,617,038 , GRCh38.p12 chr19: 12,646,620-13,506,224 DHPS, JUNB, 42 more genes
    nsv6291633copy number variation1nstd102humanPathogenic GRCh37 chr19: 12,697,728-14,111,313 , GRCh38.p12 chr19: 12,586,914-14,000,501 RN7SL619P, MIR6515, 67 more genes
    nsv6133689copy number variation1nstd213human GRCh37 chr19: 11,220,000-13,700,001 , GRCh38.p12 chr19: 11,109,324-13,589,187 ACP5, GET3, 128 more genes
    nsv6133479copy number variation1nstd213human GRCh37 chr19: 7,400,000-13,280,001 , GRCh38.p12 chr19: 7,335,095-13,169,187 , ACP5, 299 more genes
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 more genes
    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
    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
    nsv4634299copy number variation1nstd183human GRCh37 chr19: 13,211,761-13,213,728 , GRCh38.p12 chr19: 13,100,947-13,102,914 TRMT1, LYL1, 1 more genes
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