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Items: 1 to 20 of 115

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141826copy number variation1nstd232human GRCh37.p13 chr19: 12,779,238-12,779,331 , GRCh38.p12 chr19: 12,668,424-12,668,517 WDR83OS, WDR83
    nsv7095468copy number variation1nstd102humanPathogenic GRCh37 chr19: 12,757,434-12,780,217 , GRCh38.p12 chr19: 12,646,620-12,669,403 MAN2B1, WDR83, 1 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
    nsv7095268copy number variation1nstd102humanPathogenic GRCh37 chr19: 12,775,596-12,777,525 , GRCh38.p12 chr19: 12,664,782-12,666,711 MAN2B1, WDR83, 1 more genes
    nsv7095267copy number variation1nstd102humanPathogenic GRCh37 chr19: 12,768,857-12,780,217 , GRCh38.p12 chr19: 12,658,043-12,669,403 MAN2B1, WDR83, 1 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
    nsv7017420copy number variation1nstd229human GRCh38 chr19: 12,663,401-12,677,200 , GRCh37.p13 chr19: 12,774,215-12,788,014 MAN2B1, WDR83OS, 2 more genes
    nsv7016648copy number variation1nstd229human GRCh38 chr19: 12,670,873-12,671,040 , GRCh37.p13 chr19: 12,781,687-12,781,854 WDR83OS, DHPS, 1 more genes
    nsv7011234copy number variation1nstd229human GRCh38 chr19: 12,616,100-12,683,485 , GRCh37.p13 chr19: 12,726,914-12,794,299 DHPS, ZNF791, 5 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
    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
    nsv6310445copy number variation1nstd102humanUncertain significance GRCh37 chr19: 12,772,054-12,777,515 , GRCh38.p12 chr19: 12,661,240-12,666,701 WDR83, WDR83OS, 1 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
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