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Items: 1 to 20 of 108

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6716772copy number variation1nstd229human GRCh38 chr3: 49,140,954-49,160,821 , GRCh37.p13 chr3: 49,178,387-49,198,254 LAMB2P1, CCDC71
    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
    nsv6699775copy number variation1nstd229human GRCh38 chr3: 49,152,202-49,154,971 , GRCh37.p13 chr3: 49,189,635-49,192,404 LAMB2P1
    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
    nsv6366290copy number variation1nstd223human GRCh38 chr3: 49,152,411-49,156,159 , GRCh37.p13 chr3: 49,189,844-49,193,592 LAMB2P1
    nsv6363895copy number variation1nstd223human GRCh38 chr3: 49,150,640-49,151,354 , GRCh37.p13 chr3: 49,188,073-49,188,787 LAMB2P1
    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
    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
    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
    nsv4914311copy number variation1nstd200human GRCh38 chr3: 49,150,554-49,151,478 , GRCh37.p13 chr3: 49,187,987-49,188,911 LAMB2P1
    nsv4914310copy number variation1nstd200human GRCh38 chr3: 49,147,906-49,156,190 , GRCh37.p13 chr3: 49,185,339-49,193,623 LAMB2P1
    nsv4911233copy number variation1nstd200human GRCh38 chr3: 49,151,427-49,155,958 , GRCh37.p13 chr3: 49,188,860-49,193,391 LAMB2P1
    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
    nsv4728146copy number variation1nstd102humanPathogenic GRCh37 chr3: 48,807,193-51,363,558 , GRCh38.p12 chr3: 48,769,760-51,326,127 APEH, MIR5193, 90 more genes
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