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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4924382copy number variation1nstd200human GRCh38 chr3: 44,759,215-44,881,079 , GRCh37.p13 chr3: 44,800,707-44,922,571 MIR564, KIF15, 5 more genes
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4674744copy number variation1nstd102humanUncertain significance GRCh37 chr3: 44,444,902-45,413,927 , GRCh38.p12 chr3: 44,403,410-45,372,435 RPL12P44, TMEM42, 37 more genes
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 NDUFB4, LOC105374108, 2876 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 RNU4-62P, SEMA3B-AS1, 2880 more genes
    nsv3885169copy number variation1nstd102humanPathogenic GRCh37 chr3: 16,923,595-45,249,923 , GRCh38.p12 chr3: 16,884,818-45,208,431 RNU6-243P, ZNF385D, 382 more genes
    nsv3883164copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 37,028,313-49,929,220 , GRCh38.p12 chr3: 36,986,822-49,891,787 ACAA1, ACVR2B, 344 more genes
    nsv3880617copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391 RPL23AP49, DLEC1, 2875 more genes
    nsv3168877copy number variation1nstd158human GRCh37 chr3: 38,483,456-71,473,806 , GRCh38.p12 chr3: 38,441,965-71,424,655 , ACVR2B, 646 more genes
    nsv3131302copy number variation2nstd151human GRCh37 chr3: 44,839,323-46,026,407 , GRCh38.p12 chr3: 44,797,831-45,984,915 , KIF15, 30 more genes
    nsv3120994copy number variation1nstd151human GRCh37 chr3: 44,438,232-46,723,093 , GRCh38.p12 chr3: 44,396,740-46,681,603 , CCR1, 73 more genes
    nsv3119805copy number variation1nstd151human GRCh37 chr3: 44,905,686-45,000,933 , GRCh38.p12 chr3: 44,864,194-44,959,441 , GRCh38.p12 chr3|NW_009646197.1: 389,544-451,168 RPL12P44, TMEM42, 3 more genes
    nsv2768229copy-neutral loss of heterozygosity1nstd125human GRCh37 chr3: 39,873,604-53,004,620 , GRCh38.p12 chr3: 39,832,113-52,970,604 , ACY1, 400 more genes
    nsv2168049short tandem repeat1nstd128human GRCh37 chr3: 44,902,479-44,902,500 , GRCh38.p12 chr3: 44,860,987-44,861,008 , GRCh38.p12 chr3|NW_009646197.1: 386,337-386,358 TMEM42, MIR564
    nsv2164248short tandem repeat5nstd128human GRCh37 chr3: 44,907,538-44,907,584 , GRCh38.p12 chr3: 44,866,046-44,866,092 , GRCh38.p12 chr3|NW_009646197.1: 391,396-391,442 TMEM42
    nsv2164247short tandem repeat4nstd128human GRCh37 chr3: 44,903,641-44,903,657 , GRCh38.p12 chr3: 44,862,149-44,862,165 , GRCh38.p12 chr3|NW_009646197.1: 387,499-387,515 TMEM42, MIR564
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