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Items: 1 to 20 of 223

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7058723inversion1nstd229human GRCh38 chr19: 13,672,973-14,832,292 , GRCh37.p13 chr19: 13,783,787-14,943,104 SNRPGP15, NDUFB7, 53 more genes
    nsv7009275copy number variation1nstd229human GRCh38 chr19: 13,836,899-14,088,244 , GRCh37.p13 chr19: 13,947,713-14,199,056 NANOS3, RLN3, 17 more genes
    nsv7008155copy number variation1nstd229human GRCh38 chr19: 13,988,718-13,988,818 , GRCh37.p13 chr19: 14,099,530-14,099,630 RFX1
    nsv6599077inversion1nstd223human GRCh38 chr19: 12,342,953-19,691,233 , GRCh37.p13 chr19: 12,453,767-19,802,042 GET3, BST2, 314 more genes
    nsv6532940copy number variation1nstd223human GRCh38 chr19: 13,996,741-13,999,767 , GRCh37.p13 chr19: 14,107,553-14,110,579 RFX1
    nsv6291633copy number variation1nstd102humanPathogenic GRCh37 chr19: 12,697,728-14,111,313 , GRCh38.p12 chr19: 12,586,914-14,000,501 RN7SL619P, MIR6515, 67 more genes
    nsv6145391copy number variation1nstd206human GRCh38 chr19: 13,988,718-13,988,818 , GRCh37.p13 chr19: 14,099,530-14,099,630 , RFX1
    nsv6144620copy number variation1nstd206human GRCh38 chr19: 13,990,000-14,000,000 , GRCh37.p13 chr19: 14,100,812-14,110,812 , RFX1
    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
    nsv6133467copy number variation1nstd213human GRCh37 chr19: 14,110,000-14,470,001 , GRCh38.p12 chr19: 13,999,188-14,359,189 SAMD1, EEF1DP1, 14 more genes
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 more genes
    nsv5947075copy number variation1nstd209human GRCh38 chr19: 13,996,837-13,999,788 , GRCh37.p13 chr19: 14,107,649-14,110,600 , RFX1
    nsv5885544copy number variation1nstd209human GRCh38 chr19: 13,996,809-13,999,758 , GRCh37.p13 chr19: 14,107,621-14,110,570 , RFX1
    nsv5712021mobile element insertion1nstd211human GRCh38 chr19: 13,994,904-13,994,904 , GRCh37.p13 chr19: 14,105,716-14,105,716 , RFX1
    nsv5552535insertion1nstd206human GRCh38 chr19: 13,971,736-13,971,772 , GRCh37.p13 chr19: 14,082,548-14,082,584 RFX1
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