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Items: 1 to 20 of 237

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145818insertion1nstd232human GRCh37.p13 chr19: 14,944,700-14,944,700 , GRCh38.p12 chr19: 14,833,888-14,833,888 OR7A5, OR7C1
    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
    nsv7061983inversion1nstd229human GRCh38 chr19: 14,806,496-14,811,432 , GRCh37.p13 chr19: 14,917,308-14,922,244 OR7C1
    nsv7060542inversion1nstd229human GRCh38 chr19: 12,342,956-19,691,233 , GRCh37.p13 chr19: 12,453,770-19,802,042 DDX39A, KCNN1, 314 more genes
    nsv7059951inversion1nstd229human GRCh38 chr19: 14,811,108-14,817,994 , GRCh37.p13 chr19: 14,921,920-14,928,806 OR7C1
    nsv7059139inversion1nstd229human GRCh38 chr19: 12,641,624-19,910,103 , GRCh37.p13 chr19: 12,752,438-20,020,912 NR2F6, ISCA1P5, 307 more genes
    nsv7058723inversion1nstd229human GRCh38 chr19: 13,672,973-14,832,292 , GRCh37.p13 chr19: 13,783,787-14,943,104 SNRPGP15, NDUFB7, 53 more genes
    nsv7016380copy number variation1nstd229human GRCh38 chr19: 14,802,701-14,812,900 , GRCh37.p13 chr19: 14,913,513-14,923,712 OR7C1
    nsv7016274copy number variation1nstd229human GRCh38 chr19: 14,810,857-14,811,692 , GRCh37.p13 chr19: 14,921,669-14,922,504 OR7C1
    nsv7013901copy number variation1nstd229human GRCh38 chr19: 14,805,101-14,812,200 , GRCh37.p13 chr19: 14,915,913-14,923,012 OR7C1
    nsv7011191copy number variation1nstd229human GRCh38 chr19: 14,802,801-14,812,100 , GRCh37.p13 chr19: 14,913,613-14,922,912 OR7C1
    nsv7010272copy number variation1nstd229human GRCh38 chr19: 14,830,338-14,838,733 , GRCh37.p13 chr19: 14,941,150-14,949,545 OR7A5, OR7C1
    nsv7009868copy number variation1nstd229human GRCh38 chr19: 14,833,888-14,833,995 , GRCh37.p13 chr19: 14,944,700-14,944,807 OR7C1, OR7A5
    nsv7009783copy number variation1nstd229human GRCh38 chr19: 14,804,501-14,813,100 , GRCh37.p13 chr19: 14,915,313-14,923,912 OR7C1
    nsv7009514copy number variation1nstd229human GRCh38 chr19: 14,803,401-14,812,100 , GRCh37.p13 chr19: 14,914,213-14,922,912 OR7C1
    nsv7008290copy number variation1nstd229human GRCh38 chr19: 14,804,474-14,812,143 , GRCh37.p13 chr19: 14,915,286-14,922,955 OR7C1
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