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Items: 1 to 20 of 137

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5915656copy number variation1nstd209human GRCh38 chr10: 73,757,699-73,757,819 , GRCh37.p13 chr10: 75,517,457-75,517,577 SEC24C
    nsv5909992copy number variation1nstd209human GRCh38 chr10: 72,964,663-80,533,256 , GRCh37.p13 chr10: 74,724,421-82,293,012 , PRXL2A, 155 more genes
    nsv5480074copy number variation1nstd206human GRCh38 chr10: 73,757,621-73,757,720 , GRCh37.p13 chr10: 75,517,379-75,517,478 SEC24C
    nsv5477221copy number variation1nstd206human GRCh38 chr10: 73,745,705-73,747,928 , GRCh37.p13 chr10: 75,505,463-75,507,686 SEC24C
    nsv5301974copy number variation1nstd204human GRCh38.p13 chr10: 73,709,242-74,768,785 , GRCh37.p13 chr10: 75,469,000-76,528,543 , RPSAP6, 24 more genes
    nsv5247572copy number variation1nstd204human GRCh38.p13 chr10: 73,742,427-73,776,263 , GRCh37.p13 chr10: 75,502,185-75,536,021 FUT11, SEC24C
    nsv5245217copy number variation1nstd204human GRCh37.p13 chr10: 75,466,395-75,515,313 , GRCh38.p13 chr10: 73,706,637-73,755,555 GLUD1P3, SEC24C, 4 more genes
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4976538copy number variation1nstd200human GRCh38 chr10: 73,756,069-73,757,080 , GRCh37.p13 chr10: 75,515,827-75,516,838 SEC24C
    nsv4976537copy number variation1nstd200human GRCh38 chr10: 73,747,557-73,748,631 , GRCh37.p13 chr10: 75,507,315-75,508,389 SEC24C
    nsv4973773copy number variation1nstd200human GRCh38 chr10: 73,754,139-73,755,582 , GRCh37.p13 chr10: 75,513,897-75,515,340 SEC24C
    nsv4973772copy number variation1nstd200human GRCh38 chr10: 73,709,251-74,768,777 , GRCh37.p13 chr10: 75,469,009-76,528,535 , AP3M1, 24 more genes
    nsv4973771copy number variation1nstd200human GRCh38 chr10: 73,673,558-73,872,096 , GRCh37.p13 chr10: 75,433,316-75,631,854 FUT11, CAMK2G, 12 more genes
    nsv4849090copy number variation1nstd200human GRCh37 chr10: 75,507,369-75,508,364 , GRCh38.p12 chr10: 73,747,611-73,748,606 SEC24C
    nsv4839922copy number variation1nstd200human GRCh37 chr10: 75,469,009-76,528,535 , GRCh38.p12 chr10: 73,709,251-74,768,777 , NDUFA8P1, 24 more genes
    nsv4837163copy number variation1nstd200human GRCh37 chr10: 75,505,451-75,507,220 , GRCh38.p12 chr10: 73,745,693-73,747,462 SEC24C
    nsv4527237copy number variation1nstd166human GRCh37.p13 chr10: 75,522,617-75,522,669 , GRCh38.p12 chr10: 73,762,859-73,762,911 SEC24C
    nsv4456093copy number variation1nstd102humanUncertain significance GRCh37 chr10: 75,251,395-75,763,287 , GRCh38.p12 chr10: 73,491,637-74,003,529 ZSWIM8-AS1, PPP3CB-AS1, 23 more genes
    nsv4422261copy number variation1nstd174human GRCh37 chr10: 75,475,447-75,682,321 , GRCh38.p12 chr10: 73,715,689-73,922,563 GLUD1P3, ZSWIM8, 12 more genes
    nsv4343722sequence alteration1nstd166human GRCh37.p13 chr10: 43,905,894-92,001,956 , GRCh38.p12 chr10: 43,410,446-90,242,199 , ALOX5, 749 more genes
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