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Items: 1 to 20 of 170

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074210inversion1nstd229human GRCh38 chr18: 45,861,287-52,164,943 , GRCh37.p13 chr18: 43,441,252-49,691,313 LOC105372100, RNA5SP458, 103 more genes
    nsv7065765inversion1nstd229human GRCh38 chr18: 46,426,327-48,440,063 , GRCh37.p13 chr18: 44,006,290-45,966,434 ZBTB7C, MIR4527, 29 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
    nsv7060607inversion1nstd229human GRCh38 chr18: 46,563,922-48,670,215 , GRCh37.p13 chr18: 44,143,885-46,196,586 SKOR2, ELOA3DP, 32 more genes
    nsv7012068copy number variation1nstd229human GRCh38 chr18: 48,237,800-48,360,710 , GRCh37.p13 chr18: 45,764,171-45,887,081 ZBTB7C-AS2, ZBTB7C
    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
    nsv6595210inversion1nstd223human GRCh38 chr18: 47,568,608-48,389,263 , GRCh37.p13 chr18: 45,094,979-45,915,634 SMAD2, RNU6-708P, 8 more genes
    nsv6517262copy number variation1nstd223human GRCh38 chr18: 48,252,018-48,256,427 , GRCh37.p13 chr18: 45,778,389-45,782,798 ZBTB7C, ZBTB7C-AS2
    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
    nsv6290135copy number variation1nstd102humanUncertain significance GRCh37 chr18: 45,755,986-45,787,673 , GRCh38.p12 chr18: 48,229,615-48,261,302 ZBTB7C, ZBTB7C-AS2
    nsv6133446copy number variation1nstd213human GRCh37 chr18: 45,550,000-46,060,001 , GRCh38.p12 chr18: 48,023,629-48,533,630 ZBTB7C-AS2, ZBTB7C, 4 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
    nsv4676155copy number variation1nstd102humanPathogenic GRCh37 chr18: 20,689,919-49,455,212 , GRCh38.p12 chr18: 23,109,955-51,928,842 KLHL14, RPL23AP77, 318 more genes
    nsv4499657mobile element insertion1nstd166human GRCh37.p13 chr18: 45,779,233-45,779,233 , GRCh38.p12 chr18: 48,252,862-48,252,862 ZBTB7C-AS2, ZBTB7C
    nsv4457866copy number variation1nstd102humanPathogenic GRCh37 chr18: 45,621,155-61,416,536 , GRCh38.p12 chr18: 48,094,784-63,749,302 LOC105372159, LOC105372156, 208 more genes
    nsv4457507copy number variation1nstd102humanUncertain significance GRCh37 chr18: 44,619,805-46,854,791 , GRCh38.p12 chr18: 47,093,434-49,328,421 LOC105372105, CTIF, 29 more genes
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