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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
    nsv7139087copy number variation1nstd232human GRCh37.p13 chr3: 49,060,408-49,060,486 , GRCh38.p12 chr3: 49,022,975-49,023,053 IMPDH2, NDUFAF3
    nsv7096805copy number variation1nstd102humanUncertain significance GRCh37 chr3: 45,435,946-49,137,751 , GRCh38.p12 chr3: 45,394,454-49,100,318 SNORA94, LIMD1-AS1, 120 more genes
    nsv6712846copy number variation1nstd229human GRCh38 chr3: 49,020,149-49,020,180 , GRCh37.p13 chr3: 49,057,582-49,057,613 MIR191, MIR425, 2 more genes
    nsv6700836copy number variation1nstd229human GRCh38 chr3: 48,056,801-51,204,000 , GRCh37.p13 chr3: 48,098,291-51,241,431 APEH, SLC26A6, 129 more genes
    nsv6372055copy number variation1nstd223human GRCh38 chr3: 48,386,801-49,230,000 , GRCh37.p13 chr3: 48,428,291-49,267,433 NCKIPSD, UCN2, 44 more genes
    nsv6360141copy number variation1nstd223human GRCh38 chr3: 49,019,228-49,019,765 , GRCh37.p13 chr3: 49,056,661-49,057,198 MIR191, MIR425, 2 more genes
    nsv6315166copy number variation1nstd102humanPathogenic GRCh37 chr3: 44,948,482-49,115,809 , GRCh38.p12 chr3: 44,906,990-49,078,376 TMEM89, TGM4, 129 more genes
    nsv6313476copy number variation1nstd102humanUncertain significance GRCh37 chr3: 49,060,512-49,678,685 , GRCh38.p12 chr3: 49,023,079-49,641,252 DAG1, GPX1, 23 more genes
    nsv6135016copy number variation1nstd213human GRCh37 chr3: 48,760,000-52,290,001 , GRCh38.p12 chr3: 48,722,567-52,255,985 ACY1, ALAS1, 128 more genes
    nsv6134694copy number variation1nstd213human GRCh37 chr3: 46,170,000-52,140,001 , GRCh38.p12 chr3: 46,128,508-52,105,985 ACY1, AMT, 210 more genes
    nsv5906967copy number variation1nstd209human GRCh38 chr3: 49,023,953-49,024,007 , GRCh37.p13 chr3: 49,061,386-49,061,440 NDUFAF3, IMPDH2
    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
    nsv5452991copy number variation1nstd206human GRCh38 chr3: 49,023,958-49,024,008 , GRCh37.p13 chr3: 49,061,391-49,061,441 IMPDH2, NDUFAF3
    nsv5302571copy number variation1nstd204human GRCh38.p13 chr3: 49,022,280-49,022,626 , GRCh37.p13 chr3: 49,059,713-49,060,059 NDUFAF3, IMPDH2
    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
    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
    nsv4914308copy number variation1nstd200human GRCh38 chr3: 49,022,285-49,022,623 , GRCh37.p13 chr3: 49,059,718-49,060,056 NDUFAF3, IMPDH2
    nsv4914307copy number variation1nstd200human GRCh38 chr3: 49,019,218-49,019,777 , GRCh37.p13 chr3: 49,056,651-49,057,210 MIR425, MIR191, 2 more genes
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