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Items: 1 to 20 of 149

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5897039copy number variation1nstd209human GRCh38 chr3: 48,667,261-48,667,824 , GRCh37.p13 chr3: 48,704,694-48,705,257 LINC02585, NCKIPSD
    nsv5673729copy number variation1nstd102humanPathogenic GRCh37 chr3: 48,507,870-50,340,407 , GRCh38.p12 chr3: 48,466,471-50,302,976 SEMA3B-AS1, GNAT1, 87 more genes
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5452929copy number variation1nstd206human GRCh38 chr3: 48,668,735-48,668,808 , GRCh37.p13 chr3: 48,706,168-48,706,241 NCKIPSD, LINC02585
    nsv5449623copy number variation1nstd206human GRCh38 chr3: 48,667,219-48,667,800 , GRCh37.p13 chr3: 48,704,652-48,705,233 LINC02585, NCKIPSD
    nsv5443782copy number variation1nstd206human GRCh38 chr3: 48,684,094-48,684,242 , GRCh37.p13 chr3: 48,721,527-48,721,675 NCKIPSD
    nsv5211134copy number variation1nstd204human GRCh38.p13 chr3: 48,639,801-49,381,300 , GRCh37.p13 chr3: 48,677,234-49,418,733 MIR6890, IHO1, 31 more genes
    nsv5068778mobile element insertion1nstd203human GRCh38 chr3: 48,667,661-48,667,682 , GRCh37.p13 chr3: 48,705,094-48,705,115 NCKIPSD, LINC02585
    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
    nsv4924427copy number variation1nstd200human GRCh38 chr3: 48,667,191-48,668,026 , GRCh37.p13 chr3: 48,704,624-48,705,459 LINC02585, NCKIPSD
    nsv4911209copy number variation1nstd200human GRCh38 chr3: 48,675,450-48,675,588 , GRCh37.p13 chr3: 48,712,883-48,713,021 NCKIPSD
    nsv4911208copy number variation1nstd200human GRCh38 chr3: 48,672,390-48,672,508 , GRCh37.p13 chr3: 48,709,823-48,709,941 NCKIPSD
    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
    nsv4674083copy number variation1nstd102humanPathogenic GRCh37 chr3: 48,346,677-49,630,228 , GRCh38.p12 chr3: 48,305,187-49,592,795 MIR6823, NCKIPSD, 59 more genes
    nsv4586195copy number variation1nstd183human GRCh37 chr3: 48,716,419-48,716,715 , GRCh38.p12 chr3: 48,678,986-48,679,282 NCKIPSD
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4470971mobile element insertion1nstd166human GRCh37.p13 chr3: 48,718,287-48,718,287 , GRCh38.p12 chr3: 48,680,854-48,680,854 NCKIPSD
    nsv4347762copy number variation1nstd102humanPathogenic GRCh37 chr3: 45,153,770-53,878,616 , GRCh38.p12 chr3: 45,112,278-53,844,589 UQCRC1, DHX30, 291 more genes
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