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Items: 1 to 20 of 320

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098925copy number variation1nstd102humanPathogenic GRCh38 chr19: 15,014,099-16,261,691 , GRCh37.p13 chr19: 15,124,911-16,372,502 CYP4F12, OR1AB1P, 52 more genes
    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
    nsv7095270copy number variation1nstd102humanPathogenic GRCh37 chr19: 15,366,088-15,368,004 , GRCh38.p12 chr19: 15,255,277-15,257,193 BRD4
    nsv7095193copy number variation1nstd102humanUncertain significance GRCh37 chr19: 15,349,188-15,379,873 , GRCh38.p12 chr19: 15,238,377-15,269,062 BRD4
    nsv7093178copy number variation1nstd102humanUncertain significance GRCh38 chr19: 15,243,100-15,243,150 , GRCh37 chr19: 15,353,911-15,353,961 BRD4
    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
    nsv7017250copy number variation1nstd229human GRCh38 chr19: 15,306,097-15,306,584 , GRCh37.p13 chr19: 15,416,908-15,417,395 BRD4
    nsv7016822copy number variation1nstd229human GRCh38 chr19: 15,278,083-15,281,996 , GRCh37.p13 chr19: 15,388,894-15,392,807 BRD4
    nsv7015605copy number variation1nstd229human GRCh38 chr19: 15,252,103-15,295,724 , GRCh37.p13 chr19: 15,362,914-15,406,535 BRD4
    nsv7010633copy number variation1nstd229human GRCh38 chr19: 15,264,696-15,265,036 , GRCh37.p13 chr19: 15,375,507-15,375,847 BRD4
    nsv7008157copy number variation1nstd229human GRCh38 chr19: 15,311,249-15,315,833 , GRCh37.p13 chr19: 15,422,060-15,426,644 BRD4
    nsv7007884copy number variation1nstd229human GRCh38 chr19: 15,309,001-15,315,900 , GRCh37.p13 chr19: 15,419,812-15,426,711 BRD4
    nsv7007672copy number variation1nstd229human GRCh38 chr19: 15,312,388-15,315,582 , GRCh37.p13 chr19: 15,423,199-15,426,393 BRD4
    nsv7006229copy number variation1nstd229human GRCh38 chr19: 15,316,918-15,322,812 , GRCh37.p13 chr19: 15,427,729-15,433,623 BRD4
    nsv7004701copy number variation1nstd229human GRCh38 chr19: 15,300,011-15,302,081 , GRCh37.p13 chr19: 15,410,822-15,412,892 BRD4
    nsv7003086copy number variation1nstd229human GRCh38 chr19: 15,271,909-15,271,965 , GRCh37.p13 chr19: 15,382,720-15,382,776 BRD4
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