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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143702insertion1nstd232human GRCh37.p13 chr2: 14,414,607-14,414,607 , GRCh38.p12 chr2: 14,274,483-14,274,483 LINC00276, RNU6-1288P
    nsv7051990inversion1nstd229human GRCh38 chr2: 14,261,554-14,261,605 , GRCh37.p13 chr2: 14,401,678-14,401,729 LINC00276
    nsv7045205inversion1nstd229human GRCh38 chr2: 14,233,942-14,234,138 , GRCh37.p13 chr2: 14,374,066-14,374,262 LINC00276
    nsv7043330inversion1nstd229human GRCh38 chr2: 14,338,906-14,346,207 , GRCh37.p13 chr2: 14,479,030-14,486,331 LINC00276
    nsv7038983inversion1nstd229human GRCh38 chr2: 14,253,290-14,253,336 , GRCh37.p13 chr2: 14,393,414-14,393,460 LINC00276
    nsv6677914copy number variation1nstd229human GRCh38 chr2: 14,330,825-14,333,610 , GRCh37.p13 chr2: 14,470,949-14,473,734 LINC00276
    nsv6677203copy number variation1nstd229human GRCh38 chr2: 14,230,801-14,232,700 , GRCh37.p13 chr2: 14,370,925-14,372,824 LINC00276
    nsv6676456copy number variation1nstd229human GRCh38 chr2: 14,161,701-14,592,100 , GRCh37.p13 chr2: 14,301,826-14,732,224 RNU6-1288P, LINC00276
    nsv6676218copy number variation1nstd229human GRCh38 chr2: 14,345,730-14,345,989 , GRCh37.p13 chr2: 14,485,854-14,486,113 LINC00276
    nsv6676182copy number variation1nstd229human GRCh38 chr2: 14,364,729-14,364,873 , GRCh37.p13 chr2: 14,504,853-14,504,997 LINC00276
    nsv6675239copy number variation1nstd229human GRCh38 chr2: 14,360,223-14,360,307 , GRCh37.p13 chr2: 14,500,347-14,500,431 LINC00276
    nsv6674767copy number variation1nstd229human GRCh38 chr2: 14,327,185-14,327,573 , GRCh37.p13 chr2: 14,467,309-14,467,697 LINC00276
    nsv6674399copy number variation1nstd229human GRCh38 chr2: 14,173,701-14,253,500 , GRCh37.p13 chr2: 14,313,826-14,393,624 LINC00276
    nsv6673478copy number variation1nstd229human GRCh38 chr2: 14,391,175-14,391,496 , GRCh37.p13 chr2: 14,531,299-14,531,620 LINC00276
    nsv6673426copy number variation1nstd229human GRCh38 chr2: 13,894,008-14,407,201 , GRCh37.p13 chr2: 14,034,133-14,547,325 LINC00276, RNU6-1288P, 1 more genes
    nsv6670478copy number variation1nstd229human GRCh38 chr2: 14,326,899-14,378,374 , GRCh37.p13 chr2: 14,467,023-14,518,498 LINC00276
    nsv6668794copy number variation1nstd229human GRCh38 chr2: 14,282,200-14,282,426 , GRCh37.p13 chr2: 14,422,324-14,422,550 LINC00276
    nsv6665610copy number variation1nstd229human GRCh38 chr2: 14,318,322-14,320,685 , GRCh37.p13 chr2: 14,458,446-14,460,809 LINC00276
    nsv6664933copy number variation1nstd229human GRCh38 chr2: 14,312,247-14,315,135 , GRCh37.p13 chr2: 14,452,371-14,455,259 LINC00276
    nsv6661824copy number variation1nstd229human GRCh38 chr2: 14,171,770-14,472,071 , GRCh37.p13 chr2: 14,311,895-14,612,195 RNU6-1288P, LINC00276
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