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Items: 1 to 20 of 292

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7073674inversion1nstd229human GRCh38 chr13: 19,051,673-20,424,293 , GRCh37.p13 chr13: 19,625,813-20,998,432 ST6GALNAC4P1, LINC01072, 35 more genes
    nsv7071280inversion1nstd229human GRCh38 chr13: 19,060,302-19,582,752 , GRCh37.p13 chr13: 19,634,442-20,156,892 ESRRAP1, GOLM2P1, 18 more genes
    nsv7071034inversion1nstd229human GRCh38 chr13: 19,239,514-24,381,508 , GRCh37.p13 chr13: 19,813,654-24,955,646 BASP1P1, ZMYM5, 111 more genes
    nsv7069596inversion1nstd229human GRCh38 chr13: 19,338,874-19,796,660 , GRCh37.p13 chr13: 19,913,014-20,370,800 SLC25A15P2, MRPS31P2, 12 more genes
    nsv6937910copy number variation1nstd229human GRCh38 chr13: 19,297,001-19,302,500 , GRCh37.p13 chr13: 19,871,141-19,876,640 MRPL3P1, ANKRD26P3
    nsv6937161copy number variation1nstd229human GRCh38 chr13: 19,308,738-19,312,868 , GRCh37.p13 chr13: 19,882,878-19,887,008 ANKRD26P3
    nsv6936034copy number variation1nstd229human GRCh38 chr13: 19,285,153-19,285,528 , GRCh37.p13 chr13: 19,859,293-19,859,668 ANKRD26P3
    nsv6934567copy number variation1nstd229human GRCh38 chr13: 19,288,384-19,306,378 , GRCh37.p13 chr13: 19,862,524-19,880,518 MRPL3P1, ANKRD26P3
    nsv6934535copy number variation1nstd229human GRCh38 chr13: 19,329,729-19,329,756 , GRCh37.p13 chr13: 19,903,869-19,903,896 ANKRD26P3
    nsv6930481copy number variation1nstd229human GRCh38 chr13: 19,296,501-20,027,300 , GRCh37.p13 chr13: 19,870,641-20,601,440 ZMYM5, LINC00421, 16 more genes
    nsv6929678copy number variation1nstd229human GRCh38 chr13: 19,289,651-19,297,799 , GRCh37.p13 chr13: 19,863,791-19,871,939 ANKRD26P3
    nsv6929363copy number variation1nstd229human GRCh38 chr13: 19,343,501-19,694,600 , GRCh37.p13 chr13: 19,917,641-20,268,740 GOLM2P1, MRPS31P2, 11 more genes
    nsv6925939copy number variation1nstd229human GRCh38 chr13: 19,283,552-19,320,150 , GRCh37.p13 chr13: 19,857,692-19,894,290 MRPL3P1, ANKRD26P3
    nsv6925120copy number variation1nstd229human GRCh38 chr13: 19,289,441-19,294,488 , GRCh37.p13 chr13: 19,863,581-19,868,628 ANKRD26P3
    nsv6924593copy number variation1nstd229human GRCh38 chr13: 19,243,454-19,710,588 , GRCh37.p13 chr13: 19,817,594-20,284,728 MRPL3P1, MRPS31P2, 12 more genes
    nsv6923155copy number variation1nstd229human GRCh38 chr13: 19,301,769-19,710,590 , GRCh37.p13 chr13: 19,875,909-20,284,730 TPTE2, ESRRAP1, 12 more genes
    nsv6921269copy number variation1nstd229human GRCh38 chr13: 19,285,217-19,303,328 , GRCh37.p13 chr13: 19,859,357-19,877,468 ANKRD26P3, MRPL3P1
    nsv6921018copy number variation1nstd229human GRCh38 chr13: 19,291,601-19,294,000 , GRCh37.p13 chr13: 19,865,741-19,868,140 ANKRD26P3
    nsv6637646copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,436,287-22,089,005 , GRCh38.p12 chr13: 18,862,147-21,514,866 LOC105370104, RNU6-52P, 78 more genes
    nsv6637564copy number variation1nstd102humanUncertain significance GRCh37 chr13: 19,725,083-20,273,635 , GRCh38.p12 chr13: 19,150,943-19,699,495 TPTE2, CYCSP32, 16 more genes
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