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Items: 1 to 20 of 143

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143891copy number variation1nstd232human GRCh37.p13 chr19: 12,911,882-12,911,970 , GRCh38.p12 chr19: 12,801,068-12,801,156 PRDX2, RNASEH2A
    nsv7140233copy number variation1nstd232human GRCh37.p13 chr19: 12,918,142-12,918,230 , GRCh38.p12 chr19: 12,807,328-12,807,416 RNASEH2A
    nsv7095469copy number variation1nstd102humanUncertain significance GRCh37 chr19: 12,917,488-13,010,355 , GRCh38.p12 chr19: 12,806,674-12,899,541 RPS6P25, GCDH, 8 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
    nsv7065477inversion1nstd229human GRCh38 chr19: 12,810,637-12,812,959 , GRCh37.p13 chr19: 12,921,451-12,923,773 RNASEH2A
    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
    nsv7003193copy number variation1nstd229human GRCh38 chr19: 12,811,744-12,818,084 , GRCh37.p13 chr19: 12,922,558-12,928,898 RNASEH2A
    nsv6599077inversion1nstd223human GRCh38 chr19: 12,342,953-19,691,233 , GRCh37.p13 chr19: 12,453,767-19,802,042 GET3, BST2, 314 more genes
    nsv6598506inversion1nstd223human GRCh38 chr19: 12,810,724-12,811,701 , GRCh37.p13 chr19: 12,921,538-12,922,515 RNASEH2A
    nsv6595604inversion1nstd223human GRCh38 chr19: 12,810,782-12,812,771 , GRCh37.p13 chr19: 12,921,596-12,923,585 RNASEH2A
    nsv6310616copy number variation2nstd102humanUncertain significance GRCh37 chr19: 12,923,877-12,924,280 , GRCh38.p12 chr19: 12,813,063-12,813,466 RNASEH2A
    nsv6310464copy number variation1nstd102humanUncertain significance GRCh37 chr19: 12,917,488-13,205,463 , GRCh38.p12 chr19: 12,806,674-13,094,649 LOC105372281, SYCE2, 18 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
    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
    nsv6193214copy number variation1nstd214human GRCh38 chr19: 12,805,734-12,805,825 , GRCh37.p13 chr19: 12,916,548-12,916,639 RNASEH2A
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