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Items: 1 to 20 of 248

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137140copy number variation1nstd102humanPathogenic GRCh37 chr18: 55,020,078-56,892,966 , GRCh38.p12 chr18: 57,352,847-59,225,734 ATP8B1-AS1, ALPK2, 33 more genes
    nsv7073526inversion1nstd229human GRCh38 chr18: 53,651,514-59,638,513 , GRCh37.p13 chr18: 51,177,884-57,305,745 MBD2, LOC105372145, 78 more genes
    nsv7063248inversion1nstd229human GRCh38 chr18: 56,708,701-59,883,923 , GRCh37.p13 chr18: 54,375,932-57,551,155 MRPL37P1, RPS26P54, 49 more genes
    nsv7007309copy number variation1nstd229human GRCh38 chr18: 58,709,678-60,869,527 , GRCh37.p13 chr18: 56,376,910-58,536,760 LOC105372156, RPLP0P12, 37 more genes
    nsv7002151copy number variation1nstd229human GRCh38 chr18: 58,224,549-60,604,523 , GRCh37.p13 chr18: 55,891,781-58,271,756 GLUD1P4, LOC105372146, 44 more genes
    nsv6637467copy number variation1nstd102humanPathogenic GRCh37 chr18: 53,624,405-78,014,123 , GRCh38.p12 chr18: 55,957,174-80,256,240 RPL9P31, LOC100422317, 277 more genes
    nsv6589329inversion1nstd223human GRCh38 chr18: 59,045,097-59,045,833 , GRCh37.p13 chr18: 56,712,329-56,713,065 OACYLP
    nsv6516006copy number variation1nstd223human GRCh38 chr18: 59,047,120-59,048,180 , GRCh37.p13 chr18: 56,714,352-56,715,412 OACYLP
    nsv6315530copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271 LOC105372145, LOC105372016, 947 more genes
    nsv6314216copy number variation1nstd102humanPathogenic GRCh37 chr18: 52,675,201-78,014,123 , GRCh38.p12 chr18: 55,007,970-80,256,240 RNA5SP461, CYB5A, 290 more genes
    nsv6314188copy number variation1nstd102humanPathogenic GRCh37 chr18: 53,309,113-78,014,123 , GRCh38.p12 chr18: 55,641,882-80,256,240 ZNF236-DT, SERPINB2, 282 more genes
    nsv6310449copy number variation3nstd102humanUncertain significance GRCh37 chr18: 55,217,944-58,039,582 , GRCh38.p12 chr18: 57,550,712-60,372,349 RNU6-567P, LOC105372146, 54 more genes
    nsv6310362copy number variation3nstd102humanPathogenic, Uncertain significance GRCh37 chr18: 55,217,944-58,040,587 , GRCh38.p12 chr18: 57,550,712-60,373,354 CCBE1, OACYLP, 54 more genes
    nsv6274774copy number variation1nstd214human GRCh38 chr18: 59,038,768-59,038,847 , GRCh37.p13 chr18: 56,706,000-56,706,079 OACYLP
    nsv6133452copy number variation1nstd213human GRCh37 chr18: 52,210,000-59,070,001 , GRCh38.p12 chr18: 54,542,768-61,402,768 ACTBP3, FECH, 98 more genes
    nsv6112815copy number variation1nstd102humanPathogenic GRCh37 chr18: 54,285,235-77,960,815 , GRCh38.p12 chr18: 56,618,004-80,202,932 RPL31P9, TRG-TCC5-1, 271 more genes
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv5381802copy number variation1nstd102humanPathogenic GRCh37 chr18: 51,925,586-78,010,032 , GRCh38.p12 chr18: 54,399,216-80,252,149 LOC105372200, LOC105372174, 298 more genes
    nsv5381190copy number variation1nstd102humanUncertain significance GRCh37 chr18: 55,225,777-56,940,458 , GRCh38.p12 chr18: 57,558,545-59,273,226 TRG-TCC6-1, RAX, 32 more genes
    nsv5375222translocation1nstd200human GRCh38 chr18: 59,042,825-59,042,825 , GRCh38 chr20: 2,824,470-2,824,470 , GRCh37.p13 chr18: 56,710,057-56,710,057 , GRCh37.p13 chr20: 2,805,116-2,805,116 OACYLP
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