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Items: 1 to 20 of 231

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099181copy number variation1nstd231human GRCh38.p12 chr1: 18,899,486-20,046,918 , GRCh37 chr1: 19,225,980-20,373,411 CAPZB, HTR6, 32 more genes
    nsv7098827copy number variation1nstd102humanPathogenic GRCh37 chr1: 4,481,271-20,530,242 , GRCh38.p12 chr1: 4,421,211-20,203,749 LOC107985467, LINC01777, 386 more genes
    nsv7095949copy number variation1nstd102humanUncertain significance GRCh37 chr1: 19,199,339-24,690,861 , GRCh38.p12 chr1: 18,872,845-24,364,371 RPL29P6, NBPF3, 156 more genes
    nsv7095496copy number variation3nstd102humanUncertain significance GRCh37 chr1: 19,199,339-22,987,879 , GRCh38.p12 chr1: 18,872,845-22,661,386 RN7SL277P, MPHOSPH6P1, 103 more genes
    nsv7049927inversion1nstd229human GRCh38 chr1: 12,447,483-21,286,051 , GRCh37.p13 chr1: 12,507,539-21,612,544 SLC25A34, RNA5SP41, 238 more genes
    nsv6646945copy number variation1nstd229human GRCh38 chr1: 19,330,101-19,335,800 , GRCh37.p13 chr1: 19,656,595-19,662,294 SLC66A1
    nsv6646944copy number variation1nstd229human GRCh38 chr1: 19,318,660-19,328,665 , GRCh37.p13 chr1: 19,645,154-19,655,159 SLC66A1
    nsv6646882copy number variation1nstd229human GRCh38 chr1: 19,332,523-19,335,330 , GRCh37.p13 chr1: 19,659,017-19,661,824 SLC66A1
    nsv6646881copy number variation1nstd229human GRCh38 chr1: 19,325,254-19,325,598 , GRCh37.p13 chr1: 19,651,748-19,652,092 SLC66A1
    nsv6646879copy number variation1nstd229human GRCh38 chr1: 19,320,657-19,321,820 , GRCh37.p13 chr1: 19,647,151-19,648,314 SLC66A1
    nsv6646878copy number variation1nstd229human GRCh38 chr1: 19,306,007-19,314,296 , GRCh37.p13 chr1: 19,632,501-19,640,790 SLC66A1, AKR7A2
    nsv6646795copy number variation1nstd229human GRCh38 chr1: 19,330,130-19,334,706 , GRCh37.p13 chr1: 19,656,624-19,661,200 SLC66A1
    nsv6646794copy number variation1nstd229human GRCh38 chr1: 19,320,704-19,321,857 , GRCh37.p13 chr1: 19,647,198-19,648,351 SLC66A1
    nsv6646589copy number variation1nstd229human GRCh38 chr1: 18,782,901-19,372,400 , GRCh37.p13 chr1: 19,109,395-19,698,894 MIR4695, AKR7A3, 15 more genes
    nsv6646415copy number variation1nstd229human GRCh38 chr1: 19,320,703-19,321,825 , GRCh37.p13 chr1: 19,647,197-19,648,319 SLC66A1
    nsv6646414copy number variation1nstd229human GRCh38 chr1: 19,320,091-19,320,792 , GRCh37.p13 chr1: 19,646,585-19,647,286 SLC66A1
    nsv6646411copy number variation1nstd229human GRCh38 chr1: 19,299,801-19,321,500 , GRCh37.p13 chr1: 19,626,295-19,647,994 RNU6-1099P, AKR7A2, 1 more genes
    nsv6625945copy number variation1nstd224human GRCh37 chr1: 19,627,931-19,650,220 , GRCh38.p12 chr1: 19,301,437-19,323,726 RNU6-1099P, SLC66A1, 1 more genes
    nsv6333755copy number variation1nstd223human GRCh38 chr1: 19,320,005-19,320,522 , GRCh37.p13 chr1: 19,646,499-19,647,016 SLC66A1
    nsv6333537copy number variation1nstd223human GRCh38 chr1: 19,332,551-19,335,315 , GRCh37.p13 chr1: 19,659,045-19,661,809 SLC66A1
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