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Items: 1 to 20 of 172

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7075574inversion1nstd229human GRCh38 chr19: 12,969,213-12,970,832 , GRCh37.p13 chr19: 13,080,027-13,081,646 DAND5
    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
    nsv6599269inversion1nstd223human GRCh38 chr19: 12,969,213-12,970,830 , GRCh37.p13 chr19: 13,080,027-13,081,644 DAND5
    nsv6599077inversion1nstd223human GRCh38 chr19: 12,342,953-19,691,233 , GRCh37.p13 chr19: 12,453,767-19,802,042 GET3, BST2, 314 more genes
    nsv6598756inversion1nstd223human GRCh38 chr19: 12,967,778-12,967,918 , GRCh37.p13 chr19: 13,078,592-13,078,732 DAND5
    nsv6535465copy number variation1nstd223human GRCh38 chr19: 12,972,263-12,973,034 , GRCh37.p13 chr19: 13,083,077-13,083,848 DAND5
    nsv6534859copy number variation1nstd223human GRCh38 chr19: 12,971,948-12,972,979 , GRCh37.p13 chr19: 13,082,762-13,083,793 DAND5
    nsv6533857copy number variation1nstd223human GRCh38 chr19: 12,972,146-12,981,786 , GRCh37.p13 chr19: 13,082,960-13,092,600 DAND5
    nsv6533203copy number variation1nstd223human GRCh38 chr19: 12,960,119-12,973,033 , GRCh37.p13 chr19: 13,070,933-13,083,847 DAND5
    nsv6524696copy number variation1nstd223human GRCh38 chr19: 12,972,963-12,974,054 , GRCh37.p13 chr19: 13,083,777-13,084,868 DAND5
    nsv6524215copy number variation1nstd223human GRCh38 chr19: 12,964,806-12,973,038 , GRCh37.p13 chr19: 13,075,620-13,083,852 DAND5
    nsv6517128copy number variation1nstd223human GRCh38 chr19: 12,964,915-12,973,046 , GRCh37.p13 chr19: 13,075,729-13,083,860 DAND5
    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
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