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Items: 1 to 20 of 79

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4456517copy number variation1nstd102humanUncertain significance GRCh37 chr4: 8,463,600-8,536,360 , GRCh38.p12 chr4: 8,461,873-8,534,633 TRMT44
    nsv4456975copy number variation1nstd102humanUncertain significance GRCh37 chr4: 8,442,959-8,463,438 , GRCh38.p12 chr4: 8,441,232-8,461,711 TRMT44
    nsv3877788copy number variation1nstd102humanUncertain significance GRCh37 chr4: 8,373,601-8,496,780 , GRCh38.p12 chr4: 8,371,874-8,495,053 TRMT44, ACOX3, 1 more genes
    nsv3883886copy number variation1nstd102humanUncertain significance GRCh37 chr4: 8,349,533-8,446,629 , GRCh38.p12 chr4: 8,347,806-8,444,902 TRMT44, RNA5SP152, 1 more genes
    nsv3883635copy number variation1nstd102humanUncertain significance GRCh37 chr4: 8,313,806-8,569,066 , GRCh38.p12 chr4: 8,312,079-8,567,339 TRMT44, RNA5SP152, 2 more genes
    nsv6290918copy number variation1nstd102humanUncertain significance GRCh37 chr4: 8,367,623-8,609,785 , GRCh38.p12 chr4: 8,365,896-8,608,058 TRMT44, GPR78, 3 more genes
    nsv3877950copy number variation1nstd102humanPathogenic GRCh37 chr4: 4,165,334-33,324,781 , GRCh38.p12 chr4: 4,163,607-33,323,159 TRMT44, LOC100418700, 353 more genes
    nsv3885762copy number variation1nstd102humanPathogenic GRCh37 chr4: 71,552-29,006,745 , GRCh38.p12 chr4: 71,660-29,005,123 TRMT44, CD38, 456 more genes
    nsv3923296copy number variation1nstd102humanPathogenic GRCh38 chr4: 72,555-28,066,309 , NCBI36 chr4: 62,447-27,677,029 , GRCh37 chr4: 72,447-28,067,931 TRMT44, OR7E99P, 446 more genes
    nsv4674378copy number variation1nstd102humanPathogenic GRCh37 chr4: 49,450-24,280,482 , GRCh38.p12 chr4: 49,556-24,278,859 TRMT44, USP17L30, 394 more genes
    nsv6315347copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-20,964,575 , GRCh38.p12 chr4: 68,453-20,962,952 TRMT44, LOC100421802, 375 more genes
    nsv6291097copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-20,587,167 , GRCh38.p12 chr4: 68,453-20,585,544 TRMT44, LOC105374479, 372 more genes
    nsv3915161copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-20,387,231 , NCBI36 chr4: 58,345-19,996,329 , GRCh38 chr4: 68,453-20,385,608 TRMT44, CTBP1-AS, 370 more genes
    nsv1398080copy number variation1nstd102humanPathogenic GRCh37 chr4: 44,020-19,796,182 , GRCh38.p12 chr4: 44,019-19,794,559 TRMT44, RPL10AP7, 366 more genes
    nsv6112747copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,598-18,912,995 , GRCh38.p12 chr4: 68,706-18,911,372 TRMT44, GPR78, 362 more genes
    nsv3915014copy number variation1nstd102humanPathogenic NCBI36 chr4: 75,040-17,097,463 , GRCh38 chr4: 85,149-17,486,742 , GRCh37 chr4: 85,040-17,488,365 TRMT44, LOC100422637, 350 more genes
    nsv3915275copy number variation1nstd102humanPathogenic GRCh37 chr4: 72,447-17,279,636 , GRCh38 chr4: 72,555-17,278,013 , NCBI36 chr4: 62,447-16,888,734 TRMT44, OR7E99P, 347 more genes
    nsv3888069copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-15,973,383 , GRCh38.p12 chr4: 68,453-15,971,760 TRMT44, RPS3AP16, 332 more genes
    nsv3917860copy number variation1nstd102humanPathogenic GRCh38 chr4: 37,335-15,869,056 , NCBI36 chr4: 27,336-15,479,777 , GRCh37 chr4: 37,336-15,870,679 TRMT44, LOC105374338, 330 more genes
    nsv3918310copy number variation1nstd102humanPathogenic GRCh38 chr4: 72,555-15,658,035 , GRCh37 chr4: 72,447-15,659,658 , NCBI36 chr4: 62,447-15,268,756 TRMT44, RN7SL589P, 323 more genes
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