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Items: 1 to 20 of 175

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144994copy number variation1nstd232human GRCh37.p13 chr19: 18,966,895-18,966,990 , GRCh38.p12 chr19: 18,856,086-18,856,181 UPF1
    nsv7140971copy number variation1nstd232human GRCh37.p13 chr19: 18,965,845-18,965,929 , GRCh38.p12 chr19: 18,855,036-18,855,120 UPF1
    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
    nsv7015184copy number variation1nstd229human GRCh38 chr19: 18,866,220-18,866,479 , GRCh37.p13 chr19: 18,977,029-18,977,288 UPF1
    nsv7013578copy number variation1nstd229human GRCh38 chr19: 18,866,084-18,885,713 , GRCh37.p13 chr19: 18,976,893-18,996,522 UPF1, CERS1, 1 more genes
    nsv7013378copy number variation1nstd229human GRCh38 chr19: 18,858,015-18,858,176 , GRCh37.p13 chr19: 18,968,824-18,968,985 UPF1
    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
    nsv7000820copy number variation1nstd229human GRCh38 chr19: 18,849,930-18,849,965 , GRCh37.p13 chr19: 18,960,739-18,960,774 UPF1
    nsv6599077inversion1nstd223human GRCh38 chr19: 12,342,953-19,691,233 , GRCh37.p13 chr19: 12,453,767-19,802,042 GET3, BST2, 314 more genes
    nsv6529253copy number variation1nstd223human GRCh38 chr19: 18,804,926-18,829,887 , GRCh37.p13 chr19: 18,915,735-18,940,696 UPF1
    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
    nsv6284501copy number variation1nstd214human GRCh38 chr19: 18,829,592-18,829,647 , GRCh37.p13 chr19: 18,940,401-18,940,456 UPF1
    nsv6226885copy number variation1nstd214human GRCh38 chr19: 18,829,592-18,829,641 , GRCh37.p13 chr19: 18,940,401-18,940,450 UPF1
    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
    nsv6102894insertion1nstd212human GRCh38 chr19: 18,829,613-18,829,613 , GRCh37.p13 chr19: 18,940,422-18,940,422 UPF1
    nsv6102553inversion1nstd212human GRCh38 chr19: 18,724,785-21,720,303 , GRCh37.p13 chr19: 18,835,595-21,903,105 , COMP, 127 more genes
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