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Items: 1 to 20 of 293

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130884insertion1nstd186human GRCh37 chr21: 10,697,897-44,966,043 , GRCh38.p12 chr21: 12,965,809-43,546,162 , APP, 533 more genes
    nsv5965857copy number variation1nstd209human GRCh38 chr21: 14,377,888-22,678,896 , GRCh37.p13 chr21: 15,750,209-24,051,216 , LOC107985508, 80 more genes
    nsv5952615copy number variation1nstd209human GRCh38 chr21: 17,600,231-17,600,280 , GRCh37.p13 chr21: 18,972,549-18,972,598 BTG3, CXADR
    nsv5539790insertion1nstd206human GRCh38 chr21: 5,227,438-39,583,816 , GRCh37.p13 chr21: 10,697,897-44,966,043 , LOC100419041, 557 more genes
    nsv5516406copy number variation1nstd206human GRCh38 chr21: 17,591,243-17,592,685 , GRCh37.p13 chr21: 18,963,561-18,965,003 CXADR, BTG3
    nsv5327053copy number variation1nstd204human GRCh38.p13 chr21: 17,595,482-17,595,662 , GRCh37.p13 chr21: 18,967,800-18,967,980 BTG3, CXADR
    nsv5325258copy number variation1nstd204human GRCh38.p13 chr21: 17,611,052-17,611,227 , GRCh37.p13 chr21: 18,983,370-18,983,545 BTG3, CXADR, 1 more genes
    nsv5029241copy number variation1nstd200human GRCh38 chr21: 17,611,062-17,611,218 , GRCh37.p13 chr21: 18,983,380-18,983,536 BTG3, CXADR, 1 more genes
    nsv5025894copy number variation1nstd200human GRCh38 chr21: 17,231,032-17,884,426 , GRCh37.p13 chr21: 18,603,350-19,256,743 , BTF3L4P1, 13 more genes
    nsv5022891copy number variation1nstd200human GRCh38 chr21: 17,612,226-17,612,282 , GRCh37.p13 chr21: 18,984,544-18,984,600 BTG3, CXADR, 1 more genes
    nsv5022890copy number variation1nstd200human GRCh38 chr21: 17,591,243-17,592,685 , GRCh37.p13 chr21: 18,963,561-18,965,003 CXADR, BTG3
    nsv4865749copy number variation1nstd200human GRCh37 chr21: 18,983,380-18,983,536 , GRCh38.p12 chr21: 17,611,062-17,611,218 , GRCh38.p12 chr21|NT_187627.1: 7,368-7,524 BTG3-AS1, BTG3, 1 more genes
    nsv4865747copy number variation1nstd200human GRCh37 chr21: 18,603,350-19,256,743 , GRCh38.p12 chr21: 17,231,032-17,884,426 , CHODL-AS1, 13 more genes
    nsv4862639copy number variation1nstd200human GRCh37 chr21: 18,984,544-18,984,600 , GRCh38.p12 chr21: 17,612,226-17,612,282 , GRCh38.p12 chr21|NT_187627.1: 8,532-8,588 CXADR, BTG3, 1 more genes
    nsv4730021copy number variation1nstd102humanPathogenic GRCh37 chr21: 14,629,063-48,090,317 , GRCh38.p12 chr21: 13,256,742-46,670,405 SLX9, LOC105372750, 619 more genes
    nsv4679058copy number variation1nstd189human GRCh37.p13 chr21: 14,468,835-48,129,895 , GRCh38.p12 chr21: 13,096,514-46,699,983 , ADARB1, 652 more genes
    nsv4676404copy number variation1nstd102humanUncertain significance GRCh37 chr21: 18,769,495-19,611,264 , GRCh38.p12 chr21: 17,397,176-18,238,947 C21orf91, CHODL, 12 more genes
    nsv4676338copy number variation1nstd102humanUncertain significance GRCh37 chr21: 17,724,268-22,219,850 , GRCh38.p12 chr21: 16,351,947-20,847,532 PPIAP22, MIR99AHG, 41 more genes
    nsv4676306copy number variation1nstd102humanPathogenic GRCh37 chr21: 15,006,457-29,325,923 , GRCh38.p12 chr21: 13,634,136-27,953,605 JAM2, LINC01549, 161 more genes
    nsv4676170copy number variation1nstd102humanPathogenic GRCh37 chr21: 15,006,457-24,522,577 , GRCh38.p12 chr21: 13,634,136-23,150,255 FDPSP6, RNU4-45P, 108 more genes
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