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Items: 1 to 20 of 237

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7072414inversion1nstd229human GRCh38 chr18: 59,526,812-66,942,199 , GRCh37.p13 chr18: 57,194,044-64,609,436 RPIAP1, LOC105372167, 77 more genes
    nsv7069827inversion1nstd229human GRCh38 chr18: 60,254,377-67,312,517 , GRCh37.p13 chr18: 57,921,610-64,979,754 RNU6-142P, TNFRSF11A, 63 more genes
    nsv7063747inversion1nstd229human GRCh38 chr18: 60,254,699-61,555,242 , GRCh37.p13 chr18: 57,921,932-59,222,475 RNU6-116P, CTBP2P3, 10 more genes
    nsv7062873inversion1nstd229human GRCh38 chr18: 60,254,705-61,563,787 , GRCh37.p13 chr18: 57,921,938-59,231,020 CTBP2P3, LOC100421385, 10 more genes
    nsv7017563copy number variation1nstd229human GRCh38 chr18: 60,249,369-60,692,171 , GRCh37.p13 chr18: 57,916,602-58,359,404 MC4R, LOC101901828, 6 more genes
    nsv7008496copy number variation1nstd229human GRCh38 chr18: 60,173,296-60,963,859 , GRCh37.p13 chr18: 57,840,529-58,631,092 LOC105372156, HMGN1P31, 8 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
    nsv6637700copy number variation1nstd102humanLikely pathogenic GRCh37 chr18: 57,894,993-58,039,760 , GRCh38.p12 chr18: 60,227,760-60,372,527 MC4R, LOC105372155
    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
    nsv6624407copy number variation1nstd224human GRCh37 chr18: 58,017,423-58,203,292 , GRCh38.p12 chr18: 60,350,190-60,536,059 MC4R, LOC101901828, 2 more genes
    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
    nsv6133673copy number variation1nstd213human GRCh37 chr18: 58,030,000-58,140,001 , GRCh38.p12 chr18: 60,362,767-60,472,768 MC4R
    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
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