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Items: 1 to 20 of 189

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7095194copy number variation1nstd102humanUncertain significance GRCh37 chr19: 16,606,542-16,606,940 , GRCh38.p12 chr19: 16,495,731-16,496,129 CALR3, C19orf44
    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
    nsv7016868copy number variation1nstd229human GRCh38 chr19: 16,481,755-16,507,748 , GRCh37.p13 chr19: 16,592,566-16,618,559 CALR3, C19orf44
    nsv7005735copy number variation1nstd229human GRCh38 chr19: 16,483,901-16,486,100 , GRCh37.p13 chr19: 16,594,712-16,596,911 CALR3
    nsv7002322copy number variation1nstd229human GRCh38 chr19: 16,474,882-16,477,107 , GRCh37.p13 chr19: 16,585,693-16,587,918 CALR3
    nsv6599877inversion1nstd223human GRCh38 chr19: 16,494,332-16,495,043 , GRCh37.p13 chr19: 16,605,143-16,605,854 C19orf44, CALR3
    nsv6599077inversion1nstd223human GRCh38 chr19: 12,342,953-19,691,233 , GRCh37.p13 chr19: 12,453,767-19,802,042 GET3, BST2, 314 more genes
    nsv6598779inversion1nstd223human GRCh38 chr19: 16,478,350-16,478,744 , GRCh37.p13 chr19: 16,589,161-16,589,555 CALR3
    nsv6598693inversion1nstd223human GRCh38 chr19: 16,479,954-16,481,594 , GRCh37.p13 chr19: 16,590,765-16,592,405 CALR3
    nsv6598401inversion1nstd223human GRCh38 chr19: 16,488,170-16,489,270 , GRCh37.p13 chr19: 16,598,981-16,600,081 CALR3
    nsv6596382inversion1nstd223human GRCh38 chr19: 16,478,472-16,478,857 , GRCh37.p13 chr19: 16,589,283-16,589,668 CALR3
    nsv6533993copy number variation1nstd223human GRCh38 chr19: 16,481,725-16,507,778 , GRCh37.p13 chr19: 16,592,536-16,618,589 C19orf44, CALR3
    nsv6519509copy number variation1nstd223human GRCh38 chr19: 16,493,770-16,494,404 , GRCh37.p13 chr19: 16,604,581-16,605,215 C19orf44, CALR3
    nsv6310290copy number variation1nstd102humanUncertain significance GRCh37 chr19: 16,601,158-16,601,401 , GRCh38.p12 chr19: 16,490,347-16,490,590 CALR3
    nsv6310289copy number variation1nstd102humanUncertain significance GRCh37 chr19: 16,593,241-16,606,940 , GRCh38.p12 chr19: 16,482,430-16,496,129 C19orf44, CALR3
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