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Items: 1 to 20 of 349

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6128671insertion1nstd186human GRCh37 chrX: 46,948,577-46,948,577 , GRCh38.p12 chrX: 47,089,178-47,089,178 RGN
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5965890insertion1nstd209human GRCh38 chrX: 47,089,178-47,089,178 , GRCh37.p13 chrX|NW_004166866.1: 338,739-338,739 , GRCh37.p13 chrX: 46,948,577-46,948,577 RGN
    nsv5960287insertion1nstd209human GRCh38 chrX: 47,089,406-47,089,406 , GRCh37.p13 chrX: 46,948,805-46,948,805 , GRCh37.p13 chrX|NW_004166866.1: 338,967-338,967 RGN
    nsv5951501insertion1nstd209human GRCh38 chrX: 47,090,921-47,090,921 , GRCh37.p13 chrX|NW_004166866.1: 340,482-340,482 , GRCh37.p13 chrX: 46,950,320-46,950,320 RGN
    nsv5882824copy number variation1nstd209human GRCh38 chrX: 44,722,720-48,672,672 , GRCh37.p13 chrX: 44,581,966-47,619,970 ZNF674-AS1, CDK16, 115 more genes
    nsv5882241copy number variation1nstd209human GRCh38 chrX: 47,086,090-47,089,436 , GRCh37.p13 chrX|NW_004166866.1: 335,651-338,997 , GRCh37.p13 chrX: 46,945,489-46,948,835 RGN, RNU6-1189P
    nsv5873682copy number variation1nstd209human GRCh38 chrX: 41,560,623-47,265,899 , GRCh37.p13 chrX: 41,419,876-47,125,298 , CTNNBL1P1, 80 more genes
    nsv5622982insertion1nstd207human GRCh38 chrX: 47,089,178-47,089,178 , GRCh37.p13 chrX|NW_004166866.1: 338,739-338,739 , GRCh37.p13 chrX: 46,948,577-46,948,577 RGN
    nsv5612596insertion1nstd207human GRCh38 chrX: 47,089,400-47,089,400 , GRCh37.p13 chrX|NW_004166866.1: 338,961-338,961 , GRCh37.p13 chrX: 46,948,799-46,948,799 RGN
    nsv5611618insertion1nstd207human GRCh38 chrX: 47,090,909-47,090,909 , GRCh37.p13 chrX: 46,950,308-46,950,308 , GRCh37.p13 chrX|NW_004166866.1: 340,470-340,470 RGN
    nsv5562478sequence alteration1nstd206human GRCh38 chrX: 45,310,830-84,506,186 , GRCh37.p13 chrX: 45,170,075-83,761,194 , AR, 649 more genes
    nsv5556729sequence alteration1nstd206human GRCh37.p13 chrX|NW_004166866.1: 111,970-469,972 , GRCh38 chrX: 46,862,409-47,356,182 , GRCh37.p13 chrX: 46,721,844-47,079,810 USP11, RGN, 16 more genes
    nsv5552343insertion1nstd206human GRCh38 chrX: 47,089,178-47,089,178 , GRCh37.p13 chrX: 46,948,577-46,948,577 , GRCh37.p13 chrX|NW_004166866.1: 338,739-338,739 RGN
    nsv5433747copy number variation1nstd206human GRCh38 chrX: 47,078,371-47,078,481 , GRCh37.p13 chrX|NW_004166866.1: 327,932-328,042 , GRCh37.p13 chrX: 46,937,770-46,937,880 RGN
    nsv5421423copy number variation1nstd206human GRCh38 chrX: 47,078,726-47,080,751 , GRCh37.p13 chrX: 46,938,125-46,940,150 , GRCh37.p13 chrX|NW_004166866.1: 328,287-330,312 RGN
    nsv5416491copy number variation1nstd206human GRCh38 chrX: 39,941,083-72,578,519 , GRCh37.p13 chrX: 39,800,337-71,530,833 , USP51, 564 more genes
    nsv5381699copy number variation1nstd102humanUncertain significance GRCh37 chrX: 46,696,536-47,436,910 , GRCh38.p12 chrX: 46,837,101-47,577,511 LINC01560, LOC105373194, 25 more genes
    nsv5376179translocation1nstd200human GRCh38 chrX: 47,078,481-47,078,481 , GRCh38 chrX: 47,078,371-47,078,371 , GRCh37.p13 chrX|NW_004166866.1: 327,932-327,932 , GRCh37.p13 chrX: 46,937,880-46,937,880 , GRCh37.p13 chrX|NW_004166866.1: 328,042-328,042 , GRCh37.p13 chrX: 46,937,770-46,937,770 RGN
    nsv5059968copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-56,457,794 , GRCh38.p12 chrX: 251,879-56,431,361 PAGE3, METTL15P3, 785 more genes
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