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Items: 1 to 20 of 117

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7041296inversion1nstd229human GRCh38 chr3: 26,495,717-29,400,966 , GRCh37.p13 chr3: 26,537,208-29,442,457 CIAO2AP1, RNU6-342P, 29 more genes
    nsv6716529copy number variation1nstd229human GRCh38 chr3: 29,254,154-29,286,576 , GRCh37.p13 chr3: 29,295,645-29,328,067 RBMS3, RBMS3-AS3
    nsv6713500copy number variation1nstd229human GRCh38 chr3: 29,232,603-29,327,220 , GRCh37.p13 chr3: 29,274,094-29,368,711 RBMS3, RBMS3-AS3
    nsv6711339copy number variation1nstd229human GRCh38 chr3: 26,974,287-30,027,565 , GRCh37.p13 chr3: 27,015,778-30,069,056 LINC01967, TPM4P2, 29 more genes
    nsv6710241copy number variation1nstd229human GRCh38 chr3: 29,150,922-29,270,005 , GRCh37.p13 chr3: 29,192,413-29,311,496 RBMS3-AS3
    nsv6551033inversion1nstd223human GRCh38 chr3: 29,276,824-29,277,046 , GRCh37.p13 chr3: 29,318,315-29,318,537 RBMS3-AS3
    nsv6547472inversion1nstd223human GRCh38 chr3: 29,276,580-29,277,314 , GRCh37.p13 chr3: 29,318,071-29,318,805 RBMS3-AS3
    nsv6369337copy number variation1nstd223human GRCh38 chr3: 29,150,917-29,270,005 , GRCh37.p13 chr3: 29,192,408-29,311,496 RBMS3-AS3
    nsv6311966copy number variation1nstd102humanPathogenic GRCh37 chr3: 16,710,965-41,275,270 , GRCh38.p12 chr3: 16,669,458-41,233,779 LOC102724104, CRIP1P2, 291 more genes
    nsv5073097mobile element insertion1nstd203human GRCh38 chr3: 29,280,363-29,280,383 , GRCh37.p13 chr3: 29,321,854-29,321,874 RBMS3-AS3, RBMS3
    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
    nsv4927041copy number variation1nstd200human GRCh38 chr3: 29,271,226-29,275,205 , GRCh37.p13 chr3: 29,312,717-29,316,696 RBMS3-AS3
    nsv4924286copy number variation1nstd200human GRCh38 chr3: 29,254,154-29,286,576 , GRCh37.p13 chr3: 29,295,645-29,328,067 RBMS3, RBMS3-AS3
    nsv4924285copy number variation1nstd200human GRCh38 chr3: 29,232,603-29,327,223 , GRCh37.p13 chr3: 29,274,094-29,368,714 RBMS3-AS3, RBMS3
    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
    nsv4674536copy number variation1nstd102humanUncertain significance GRCh37 chr3: 25,901,794-29,520,717 , GRCh38.p12 chr3: 25,860,303-29,479,226 KIAA1143P2, LINC01981, 35 more genes
    nsv4588522copy number variation1nstd183human GRCh37 chr3: 29,287,169-30,116,121 , GRCh38.p12 chr3: 29,245,678-30,074,630 , RBMS3, 4 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
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