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Items: 1 to 20 of 93

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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
    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
    nsv7065158inversion1nstd229human GRCh38 chr19: 14,460,673-15,212,288 , GRCh37.p13 chr19: 14,571,485-15,323,099 RN7SL842P, ADGRE2, 37 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
    nsv7011678copy number variation1nstd229human GRCh38 chr19: 14,836,103-14,840,685 , GRCh37.p13 chr19: 14,946,915-14,951,497 OR7A10
    nsv6599077inversion1nstd223human GRCh38 chr19: 12,342,953-19,691,233 , GRCh37.p13 chr19: 12,453,767-19,802,042 GET3, BST2, 314 more genes
    nsv6533046copy number variation1nstd223human GRCh38 chr19: 14,737,233-14,986,636 , GRCh37.p13 chr19: 14,848,045-15,097,448 OR7A18P, TMEM167AP2, 13 more genes
    nsv6532629copy number variation1nstd223human GRCh38 chr19: 14,694,493-14,844,127 , GRCh37.p13 chr19: 14,805,305-14,954,939 OR7C1, OR7A10, 4 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
    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
    nsv4676112copy number variation1nstd102humanPathogenic GRCh37 chr19: 14,368,330-15,712,368 , GRCh38.p12 chr19: 14,257,518-15,601,557 GIPC1, LOC100422106, 52 more genes
    nsv4537343copy number variation1nstd166human GRCh37.p13 chr19: 14,939,000-14,952,000 , GRCh38.p12 chr19: 14,828,188-14,841,188 OR7C1, OR7A5, 1 more genes
    nsv4503442mobile element insertion1nstd166human GRCh37.p13 chr19: 14,951,555-14,951,555 , GRCh38.p12 chr19: 14,840,743-14,840,743 OR7A10
    nsv4387718copy number variation1nstd173human GRCh37 chr19: 14,921,852-15,061,579 , GRCh38.p12 chr19: 14,811,040-14,950,767 OR7A3P, OR7A1P, 11 more genes
    nsv4260861copy number variation1nstd166human GRCh37.p13 chr19: 14,946,915-14,951,493 , GRCh38.p12 chr19: 14,836,103-14,840,681 OR7A10
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