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Items: 1 to 20 of 227

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7016645copy number variation1nstd229human GRCh38 chr18: 24,631,407-24,632,103 , GRCh37.p13 chr18: 22,211,371-22,212,067 LINC01915
    nsv7015419copy number variation1nstd229human GRCh38 chr18: 24,647,707-24,664,787 , GRCh37.p13 chr18: 22,227,671-22,244,751 LINC01915
    nsv7014433copy number variation1nstd229human GRCh38 chr18: 24,658,477-24,661,252 , GRCh37.p13 chr18: 22,238,441-22,241,216 LINC01915
    nsv7010661copy number variation1nstd229human GRCh38 chr18: 24,627,563-24,627,764 , GRCh37.p13 chr18: 22,207,527-22,207,728 LINC01915
    nsv7001485copy number variation1nstd229human GRCh38 chr18: 23,020,759-30,428,209 , GRCh37.p13 chr18: 20,600,722-28,008,175 RN7SL97P, RIOK3, 76 more genes
    nsv6624579copy number variation2nstd224human GRCh37 chr18: 22,209,970-22,290,711 , GRCh38.p12 chr18: 24,630,006-24,710,747 LOC105372027, RAC1P1, 2 more genes
    nsv6624375copy number variation1nstd224human GRCh37 chr18: 22,012,716-22,348,248 , GRCh38.p12 chr18: 24,432,752-24,768,284 LOC105372028, HRH4, 8 more genes
    nsv6624143copy number variation1nstd224human GRCh37 chr18: 22,207,589-22,290,711 , GRCh38.p12 chr18: 24,627,625-24,710,747 PPIAP57, RAC1P1, 2 more genes
    nsv6579833inversion1nstd223human GRCh38 chr18: 24,644,309-24,645,041 , GRCh37.p13 chr18: 22,224,273-22,225,005 LINC01915
    nsv6532018copy number variation1nstd223human GRCh38 chr18: 24,640,201-24,641,800 , GRCh37.p13 chr18: 22,220,165-22,221,764 LINC01915
    nsv6315530copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271 LOC105372145, LOC105372016, 947 more genes
    nsv6314722copy number variation1nstd102humanPathogenic GRCh37 chr18: 1,262,334-53,254,751 , GRCh38.p12 chr18: 1,262,333-55,587,520 LOC107985176, ZNF521, 632 more genes
    nsv6291786copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-25,252,276 , GRCh38.p12 chr18: 136,226-27,672,312 LOC107985122, LOC100130487, 375 more genes
    nsv6291540copy number variation1nstd102humanUncertain significance GRCh37 chr18: 18,611,942-26,843,691 , GRCh38.p12 chr18: 21,031,981-29,263,726 MIR133A1HG, LOC105372040, 111 more genes
    nsv6259256mobile element insertion1nstd215human GRCh38 chr18: 24,645,390-24,645,390 , GRCh37.p13 chr18: 22,225,354-22,225,354 LINC01915
    nsv6133380copy number variation1nstd213human GRCh37 chr18: 21,980,000-24,910,001 , GRCh38.p12 chr18: 24,400,036-27,330,037 NPM1P2, SS18, 39 more genes
    nsv5289997copy number variation1nstd204human GRCh38.p13 chr18: 24,637,466-24,638,615 , GRCh37.p13 chr18: 22,217,430-22,218,579 LINC01915
    nsv5288766copy number variation1nstd204human GRCh38.p13 chr18: 24,638,316-24,639,515 , GRCh37.p13 chr18: 22,218,280-22,219,479 LINC01915
    nsv5283914copy number variation1nstd204human GRCh38.p13 chr18: 24,626,118-24,627,217 , GRCh37.p13 chr18: 22,206,082-22,207,181 LINC01915
    nsv5280510copy number variation1nstd204human GRCh38.p13 chr18: 24,622,341-24,649,417 , GRCh37.p13 chr18: 22,202,305-22,229,381 LINC01915
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