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Items: 1 to 20 of 238

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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
    nsv7070273inversion1nstd229human GRCh38 chr19: 13,811,891-13,832,602 , GRCh37.p13 chr19: 13,922,705-13,943,416 MIR23AHG, RN7SL619P, 2 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
    nsv7060894inversion1nstd229human GRCh38 chr19: 13,509,347-13,828,636 , GRCh37.p13 chr19: 13,620,161-13,939,450 C19orf53, LOC107985334, 6 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
    nsv7005996copy number variation1nstd229human GRCh38 chr19: 13,725,201-13,895,200 , GRCh37.p13 chr19: 13,836,015-14,006,013 NANOS3, MIR23AHG, 12 more genes
    nsv7004269copy number variation1nstd229human GRCh38 chr19: 13,798,722-13,800,364 , GRCh37.p13 chr19: 13,909,536-13,911,178 ZSWIM4
    nsv7004018copy number variation1nstd229human GRCh38 chr19: 13,790,034-13,806,030 , GRCh37.p13 chr19: 13,900,848-13,916,844 ZSWIM4
    nsv7001767copy number variation1nstd229human GRCh38 chr19: 13,827,343-13,829,796 , GRCh37.p13 chr19: 13,938,157-13,940,610 ZSWIM4
    nsv6998227copy number variation1nstd229human GRCh38 chr19: 13,814,359-13,824,515 , GRCh37.p13 chr19: 13,925,173-13,935,329 LOC107985334, RN7SL619P, 1 more genes
    nsv6599077inversion1nstd223human GRCh38 chr19: 12,342,953-19,691,233 , GRCh37.p13 chr19: 12,453,767-19,802,042 GET3, BST2, 314 more genes
    nsv6528334copy number variation1nstd223human GRCh38 chr19: 13,827,510-13,835,108 , GRCh37.p13 chr19: 13,938,324-13,945,922 MIR27A, MIR23AHG, 3 more genes
    nsv6524781copy number variation1nstd223human GRCh38 chr19: 13,800,501-13,802,600 , GRCh37.p13 chr19: 13,911,315-13,913,414 ZSWIM4
    nsv6523146copy number variation1nstd223human GRCh38 chr19: 13,801,899-13,802,687 , GRCh37.p13 chr19: 13,912,713-13,913,501 ZSWIM4
    nsv6519279copy number variation1nstd223human GRCh38 chr19: 13,796,403-13,797,344 , GRCh37.p13 chr19: 13,907,217-13,908,158 ZSWIM4
    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
    nsv6145679copy number variation1nstd206human GRCh38 chr19: 13,790,000-13,806,000 , GRCh37.p13 chr19: 13,900,814-13,916,814 ZSWIM4
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