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Items: 1 to 20 of 179

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095477copy number variation1nstd102humanUncertain significance GRCh37 chr19: 17,927,663-19,312,528 , GRCh38.p12 chr19: 17,816,854-19,201,719 BORCS8, ARMC6, 60 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
    nsv7063889inversion1nstd229human GRCh38 chr19: 17,856,052-19,078,279 , GRCh37.p13 chr19: 17,966,861-19,189,088 REX1BD, CRLF1, 52 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
    nsv7012541copy number variation1nstd229human GRCh38 chr19: 18,752,929-19,394,687 , GRCh37.p13 chr19: 18,863,739-19,505,496 SLC25A42, NCAN, 24 more genes
    nsv7010771copy number variation1nstd229human GRCh38 chr19: 18,897,022-18,900,071 , GRCh37.p13 chr19: 19,007,831-19,010,880 COPE, CERS1
    nsv7004972copy number variation1nstd229human GRCh38 chr19: 18,904,503-18,904,992 , GRCh37.p13 chr19: 19,015,312-19,015,801 COPE
    nsv6599077inversion1nstd223human GRCh38 chr19: 12,342,953-19,691,233 , GRCh37.p13 chr19: 12,453,767-19,802,042 GET3, BST2, 314 more genes
    nsv6524879copy number variation1nstd223human GRCh38 chr19: 18,917,874-18,918,932 , GRCh37.p13 chr19: 19,028,683-19,029,741 DDX49, COPE
    nsv6310474copy number variation1nstd102humanUncertain significance GRCh37 chr19: 18,893,725-19,312,528 , GRCh38.p12 chr19: 18,782,915-19,201,719 MEF2B, SLC25A42, 16 more genes
    nsv6242833mobile element insertion1nstd215human GRCh38 chr19: 18,902,803-18,902,803 , GRCh37.p13 chr19: 19,013,612-19,013,612 COPE
    nsv6234373insertion1nstd214human GRCh38 chr19: 18,902,817-18,902,817 , GRCh37.p13 chr19: 19,013,626-19,013,626 COPE
    nsv6232785insertion3nstd214human GRCh38 chr19: 18,902,825-18,902,825 , GRCh37.p13 chr19: 19,013,634-19,013,634 COPE
    nsv6229838insertion1nstd214human GRCh38 chr19: 18,902,821-18,902,821 , GRCh37.p13 chr19: 19,013,630-19,013,630 COPE
    nsv6133400copy number variation1nstd213human GRCh37 chr19: 18,720,000-20,740,001 , GRCh38.p12 chr19: 18,609,190-20,557,195 COMP, NCAN, 81 more genes
    nsv6106683insertion1nstd212human GRCh38 chr19: 18,902,825-18,902,825 , GRCh37.p13 chr19: 19,013,634-19,013,634 COPE
    nsv6102553inversion1nstd212human GRCh38 chr19: 18,724,785-21,720,303 , GRCh37.p13 chr19: 18,835,595-21,903,105 , COMP, 127 more genes
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 more genes
    nsv5973820insertion1nstd209human GRCh38 chr19: 18,902,825-18,902,825 , GRCh37.p13 chr19: 19,013,634-19,013,634 COPE
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