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Items: 1 to 20 of 210

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139607copy number variation1nstd232human GRCh37.p13 chr18: 47,017,815-47,017,900 , GRCh38.p12 chr18: 49,491,445-49,491,530 RPL17, SNORD58B, 2 more genes
    nsv7074210inversion1nstd229human GRCh38 chr18: 45,861,287-52,164,943 , GRCh37.p13 chr18: 43,441,252-49,691,313 LOC105372100, RNA5SP458, 103 more genes
    nsv7073421inversion1nstd229human GRCh38 chr18: 49,383,488-49,489,016 , GRCh37.p13 chr18: 46,909,858-47,015,386 C18orf32, SNORD58C, 5 more genes
    nsv7064950inversion1nstd229human GRCh38 chr18: 49,426,149-50,066,271 , GRCh37.p13 chr18: 46,952,519-47,592,641 SRP72P1, C18orf32, 19 more genes
    nsv7062073inversion1nstd229human GRCh38 chr18: 42,140,183-50,368,023 , GRCh37.p13 chr18: 39,720,147-47,894,393 ACAA2, MIR4320, 105 more genes
    nsv7015620copy number variation1nstd229human GRCh38 chr18: 48,566,814-53,963,212 , GRCh37.p13 chr18: 46,093,185-51,489,582 LINC02837, RPL29P32, 65 more genes
    nsv7008134copy number variation1nstd229human GRCh38 chr18: 49,337,146-49,662,979 , GRCh37.p13 chr18: 46,863,516-47,189,349 LIPG, RPL17, 13 more genes
    nsv6998773copy number variation1nstd229human GRCh38 chr18: 44,716,377-50,773,277 , GRCh37.p13 chr18: 42,296,342-48,299,647 LOC105372101, MTCO2P2, 95 more genes
    nsv6595020inversion1nstd223human GRCh38 chr18: 49,148,101-52,144,680 , GRCh37.p13 chr18: 46,674,471-49,671,050 MYO5B, LIPG, 49 more genes
    nsv6581621inversion1nstd223human GRCh38 chr18: 49,483,986-49,487,992 , GRCh37.p13 chr18: 47,010,356-47,014,362 RPL17, C18orf32, 3 more genes
    nsv6534787copy number variation1nstd223human GRCh38 chr18: 49,466,701-49,513,500 , GRCh37.p13 chr18: 46,993,071-47,039,870 RPL17, SNORD58A, 8 more genes
    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
    nsv6310262copy number variation1nstd102humanUncertain significance GRCh37 chr18: 46,570,425-48,604,837 , GRCh38.p12 chr18: 49,044,055-51,078,467 SNORD58C, SKA1, 40 more genes
    nsv6133439copy number variation1nstd213human GRCh37 chr18: 28,680,000-49,600,001 , GRCh38.p12 chr18: 31,100,037-52,073,631 ATP5F1A, DSC1, 240 more genes
    nsv6133333copy number variation1nstd213human GRCh37 chr18: 27,400,000-52,060,001 , GRCh38.p12 chr18: 29,820,035-54,532,766 ATP5F1A, DCC, 259 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
    nsv6112018inversion1nstd212human GRCh38 chr18: 47,665,415-49,687,026 , GRCh37.p13 chr18: 45,191,786-47,213,396 , SMAD2, 34 more genes
    nsv5969313inversion1nstd209human GRCh38 chr18: 49,148,257-52,144,553 , GRCh37.p13 chr18: 46,674,627-49,670,923 , SMAD4, 52 more genes
    nsv5380557translocation1nstd200human GRCh38 chr1: 29,343,715-29,343,715 , GRCh38 chr18: 49,487,234-49,487,234 , GRCh37.p13 chr1: 29,670,227-29,670,227 , GRCh37.p13 chr18: 47,013,604-47,013,604 RPL17, C18orf32, 3 more genes
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