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Items: 1 to 20 of 127

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7051368inversion1nstd229human GRCh38 chr6: 20,052,222-24,804,874 , GRCh37.p13 chr6: 20,052,453-24,805,102 LOC102724736, LOC105374966, 51 more genes
    nsv6797052copy number variation1nstd229human GRCh38 chr6: 24,126,414-24,135,909 , GRCh37.p13 chr6: 24,126,642-24,136,137 NRSN1
    nsv6789875copy number variation1nstd229human GRCh38 chr6: 24,131,301-24,133,900 , GRCh37.p13 chr6: 24,131,529-24,134,128 NRSN1
    nsv6785254copy number variation1nstd229human GRCh38 chr6: 24,140,275-24,143,427 , GRCh37.p13 chr6: 24,140,503-24,143,655 NRSN1
    nsv6785052copy number variation1nstd229human GRCh38 chr6: 24,134,518-24,143,173 , GRCh37.p13 chr6: 24,134,746-24,143,401 NRSN1
    nsv6780468copy number variation1nstd229human GRCh38 chr6: 24,128,267-24,128,814 , GRCh37.p13 chr6: 24,128,495-24,129,042 NRSN1
    nsv6779192copy number variation1nstd229human GRCh38 chr6: 24,124,905-24,125,748 , GRCh37.p13 chr6: 24,125,133-24,125,976 NRSN1
    nsv6563104inversion1nstd223human GRCh38 chr6: 20,052,171-24,804,275 , GRCh37.p13 chr6: 20,052,402-24,804,503 HDGFL1, LOC105374976, 51 more genes
    nsv6414051copy number variation1nstd223human GRCh38 chr6: 22,758,890-24,281,499 , GRCh37.p13 chr6: 22,759,119-24,281,727 DCDC2, RPL6P18, 10 more genes
    nsv6407425copy number variation1nstd223human GRCh38 chr6: 24,123,101-24,128,500 , GRCh37.p13 chr6: 24,123,329-24,128,728 NRSN1
    nsv6399126copy number variation1nstd223human GRCh38 chr6: 24,125,901-24,126,600 , GRCh37.p13 chr6: 24,126,129-24,126,828 NRSN1
    nsv6267932copy number variation1nstd214human GRCh38 chr6: 24,134,779-24,134,857 , GRCh37.p13 chr6: 24,135,007-24,135,085 NRSN1
    nsv5899208copy number variation1nstd209human GRCh38 chr6: 24,134,779-24,134,857 , GRCh37.p13 chr6: 24,135,007-24,135,085 NRSN1
    nsv5468896copy number variation1nstd206human GRCh38 chr6: 24,134,779-24,134,858 , GRCh37.p13 chr6: 24,135,007-24,135,086 NRSN1
    nsv5378298translocation1nstd200human GRCh38 chr6: 24,134,779-24,134,779 , GRCh38 chr6: 24,134,858-24,134,858 , GRCh37.p13 chr6: 24,135,086-24,135,086 , GRCh37.p13 chr6: 24,135,007-24,135,007 NRSN1
    nsv4940411copy number variation1nstd200human GRCh38 chr6: 24,139,877-24,141,574 , GRCh37.p13 chr6: 24,140,105-24,141,802 NRSN1
    nsv4934519copy number variation1nstd200human GRCh38 chr6: 24,064,628-24,179,802 , GRCh37.p13 chr6: 24,064,856-24,180,030 NRSN1, DCDC2
    nsv4815629copy number variation1nstd200human GRCh37 chr6: 24,140,105-24,141,802 , GRCh38.p12 chr6: 24,139,877-24,141,574 NRSN1
    nsv4815628copy number variation1nstd200human GRCh37 chr6: 24,135,007-24,135,086 , GRCh38.p12 chr6: 24,134,779-24,134,858 NRSN1
    nsv4483205mobile element insertion1nstd166human GRCh37.p13 chr6: 24,125,515-24,125,515 , GRCh38.p12 chr6: 24,125,287-24,125,287 NRSN1
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