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Items: 1 to 20 of 125

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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
    nsv7064525inversion1nstd229human GRCh38 chr19: 15,479,233-16,002,161 , GRCh37.p13 chr19: 15,590,044-16,112,971 CLEC4OP, LOC100422106, 24 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
    nsv7006545copy number variation1nstd229human GRCh38 chr19: 15,944,511-15,969,621 , GRCh37.p13 chr19: 16,055,321-16,080,431 OR10H4
    nsv6599077inversion1nstd223human GRCh38 chr19: 12,342,953-19,691,233 , GRCh37.p13 chr19: 12,453,767-19,802,042 GET3, BST2, 314 more genes
    nsv6133691copy number variation1nstd213human GRCh37 chr19: 15,360,000-18,450,001 , GRCh38.p12 chr19: 15,249,189-18,339,191 BST2, NR2F6, 123 more genes
    nsv6133690copy number variation1nstd213human GRCh37 chr19: 13,260,000-16,840,001 , GRCh38.p12 chr19: 13,149,186-16,729,190 PRKACA, SLC1A6, 137 more genes
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 more genes
    nsv5933091copy number variation1nstd209human GRCh38 chr19: 15,945,751-15,973,640 , GRCh37.p13 chr19: 16,056,561-16,084,450 OR10H4
    nsv5876502copy number variation1nstd209human GRCh38 chr19: 15,945,683-15,973,501 , GRCh37.p13 chr19: 16,056,493-16,084,311 OR10H4
    nsv5871472copy number variation2nstd209human GRCh38 chr19: 15,946,283-15,949,482 , GRCh37.p13 chr19: 16,057,093-16,060,292 OR10H4
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv4729750copy number variation1nstd102humanPathogenic GRCh37 chr19: 14,286,624-20,956,753 , GRCh38.p12 chr19: 14,175,812-20,773,947 LOC105372309, RAB8A, 269 more genes
    nsv4628505copy number variation1nstd183human GRCh37 chr19: 15,422,142-16,172,833 , GRCh38.p12 chr19: 15,311,331-16,062,023 , CYP4F8, 36 more genes
    nsv4457713copy number variation1nstd102humanUncertain significance GRCh37 chr19: 15,623,742-16,301,544 , GRCh38.p12 chr19: 15,512,931-16,190,733 CIB3, UCA1-AS1, 34 more genes
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