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Items: 1 to 20 of 196

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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
    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
    nsv7012601copy number variation1nstd229human GRCh38 chr19: 16,153,532-16,153,594 , GRCh37.p13 chr19: 16,264,342-16,264,404 HSH2D
    nsv7010898copy number variation1nstd229human GRCh38 chr19: 16,141,255-16,145,439 , GRCh37.p13 chr19: 16,252,065-16,256,249 HSH2D
    nsv7009365copy number variation1nstd229human GRCh38 chr19: 16,152,325-16,167,740 , GRCh37.p13 chr19: 16,263,135-16,278,551 HSH2D, CIB3
    nsv7002437copy number variation1nstd229human GRCh38 chr19: 16,157,698-16,162,183 , GRCh37.p13 chr19: 16,268,509-16,272,994 HSH2D, CIB3
    nsv7001386copy number variation1nstd229human GRCh38 chr19: 16,133,506-16,133,550 , GRCh37.p13 chr19: 16,244,316-16,244,360 RAB8A, HSH2D
    nsv7000082copy number variation1nstd229human GRCh38 chr19: 16,157,086-16,157,458 , GRCh37.p13 chr19: 16,267,896-16,268,269 HSH2D
    nsv6599794inversion1nstd223human GRCh38 chr19: 16,155,821-16,156,314 , GRCh37.p13 chr19: 16,266,631-16,267,124 HSH2D
    nsv6599077inversion1nstd223human GRCh38 chr19: 12,342,953-19,691,233 , GRCh37.p13 chr19: 12,453,767-19,802,042 GET3, BST2, 314 more genes
    nsv6529831copy number variation1nstd223human GRCh38 chr19: 16,142,612-16,143,165 , GRCh37.p13 chr19: 16,253,422-16,253,975 HSH2D
    nsv6527772copy number variation1nstd223human GRCh38 chr19: 16,143,142-16,146,969 , GRCh37.p13 chr19: 16,253,952-16,257,779 HSH2D
    nsv6525487copy number variation1nstd223human GRCh38 chr19: 16,152,331-16,167,712 , GRCh37.p13 chr19: 16,263,141-16,278,523 CIB3, HSH2D
    nsv6206104copy number variation1nstd214human GRCh38 chr19: 16,153,532-16,153,593 , GRCh37.p13 chr19: 16,264,342-16,264,403 HSH2D
    nsv6193361copy number variation1nstd214human GRCh38 chr19: 16,153,999-16,154,122 , GRCh37.p13 chr19: 16,264,809-16,264,932 HSH2D
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