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Items: 1 to 20 of 387

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095297copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-5,696,788 , GRCh38.p12 chr19: 589,946-5,696,777 NCLN, RN7SL202P, 223 more genes
    nsv7095226copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-4,818,389 , GRCh38.p12 chr19: 589,946-4,818,377 ATP5F1D, LOC102723798, 204 more genes
    nsv7068649inversion1nstd229human GRCh38 chr19: 4,313,135-7,007,201 , GRCh37.p13 chr19: 4,313,132-7,007,212 CAPS, SH2D3A, 93 more genes
    nsv7067646inversion1nstd229human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , UHRF1, 192 more genes
    nsv7017810copy number variation1nstd229human GRCh38 chr19: 4,323,001-4,523,900 , GRCh37.p13 chr19: 4,322,998-4,523,912 CHAF1A, FSD1, 9 more genes
    nsv7014283copy number variation1nstd229human GRCh38 chr19: 4,509,601-4,517,800 , GRCh37.p13 chr19: 4,509,613-4,517,812 PLIN4
    nsv7013774copy number variation1nstd229human GRCh38 chr19: 4,497,442-4,532,495 , GRCh37.p13 chr19: 4,497,439-4,532,507 PLIN4, PLIN5, 1 more genes
    nsv7005209copy number variation1nstd229human GRCh38 chr19: 4,514,501-4,524,300 , GRCh37.p13 chr19: 4,514,513-4,524,312 PLIN5, PLIN4
    nsv7000875copy number variation1nstd229human GRCh38 chr19: 4,508,261-4,511,165 , GRCh37.p13 chr19: 4,508,273-4,511,177 PLIN4
    nsv6634858copy number variation1nstd227human GRCh38.p12 chr19: 4,340,745-4,575,361 , GRCh37 chr19: 4,340,742-4,575,373 SH3GL1, CHAF1A, 10 more genes
    nsv6598603inversion1nstd223human GRCh38 chr19: 4,262,367-4,610,905 , GRCh37.p13 chr19: 4,262,364-4,610,917 STAP2, FSD1, 15 more genes
    nsv6597296inversion1nstd223human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , ALKBH7, 192 more genes
    nsv6533333copy number variation1nstd223human GRCh38 chr19: 4,509,197-4,510,392 , GRCh37.p13 chr19: 4,509,209-4,510,404 PLIN4
    nsv6531688copy number variation1nstd223human GRCh38 chr19: 4,511,425-4,513,083 , GRCh37.p13 chr19: 4,511,437-4,513,095 PLIN4
    nsv6527060copy number variation1nstd223human GRCh38 chr19: 4,512,654-4,513,082 , GRCh37.p13 chr19: 4,512,666-4,513,094 PLIN4
    nsv6524938copy number variation1nstd223human GRCh38 chr19: 4,520,567-4,527,204 , GRCh37.p13 chr19: 4,520,579-4,527,216 PLIN5, PLIN4
    nsv6521606copy number variation1nstd223human GRCh38 chr19: 4,511,467-4,512,456 , GRCh37.p13 chr19: 4,511,479-4,512,468 PLIN4
    nsv6306820copy number variation1nstd186human GRCh37 chr19: 4,511,567-4,513,017 , GRCh38.p12 chr19: 4,511,555-4,513,005 PLIN4
    nsv6306400copy number variation1nstd186human GRCh37 chr19: 4,510,818-4,511,510 , GRCh38.p12 chr19: 4,510,806-4,511,498 PLIN4
    nsv6291587copy number variation1nstd102humanPathogenic GRCh37 chr19: 3,501,624-5,357,124 , GRCh38.p12 chr19: 3,501,626-5,357,113 RN7SL202P, EIF1P6, 67 more genes
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