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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098421copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 123,787,712-123,787,878 , GRCh38.p12 chr9: 121,025,434-121,025,600 C5
    nsv7073917inversion1nstd229human GRCh38 chr9: 120,993,191-121,000,588 , GRCh37.p13 chr9: 123,755,469-123,762,866 C5
    nsv7065263inversion1nstd229human GRCh38 chr9: 120,986,322-121,000,885 , GRCh37.p13 chr9: 123,748,600-123,763,163 C5
    nsv6878079copy number variation1nstd229human GRCh38 chr9: 121,028,486-121,030,168 , GRCh37.p13 chr9: 123,790,764-123,792,446 C5
    nsv6876580copy number variation1nstd229human GRCh38 chr9: 120,991,494-120,993,078 , GRCh37.p13 chr9: 123,753,772-123,755,356 C5
    nsv6875803copy number variation1nstd229human GRCh38 chr9: 120,975,731-120,977,033 , GRCh37.p13 chr9: 123,738,009-123,739,311 C5
    nsv6873148copy number variation1nstd229human GRCh38 chr9: 121,020,232-121,024,545 , GRCh37.p13 chr9: 123,782,510-123,786,823 C5
    nsv6872864copy number variation1nstd229human GRCh38 chr9: 121,046,783-121,046,828 , GRCh37.p13 chr9: 123,809,061-123,809,106 C5
    nsv6869806copy number variation1nstd229human GRCh38 chr9: 120,960,845-120,965,318 , GRCh37.p13 chr9: 123,723,123-123,727,596 C5
    nsv6868996copy number variation1nstd229human GRCh38 chr9: 121,040,184-121,101,962 , GRCh37.p13 chr9: 123,802,462-123,864,240 C5, CNTRL
    nsv6867816copy number variation1nstd229human GRCh38 chr9: 121,001,801-121,003,700 , GRCh37.p13 chr9: 123,764,079-123,765,978 C5
    nsv6866487copy number variation1nstd229human GRCh38 chr9: 120,963,000-120,963,155 , GRCh37.p13 chr9: 123,725,278-123,725,433 C5
    nsv6865765copy number variation1nstd229human GRCh38 chr9: 121,066,609-121,078,670 , GRCh37.p13 chr9: 123,828,887-123,840,948 C5, CNTRL
    nsv6864830copy number variation1nstd229human GRCh38 chr9: 120,990,501-121,000,300 , GRCh37.p13 chr9: 123,752,779-123,762,578 C5
    nsv6863675copy number variation1nstd229human GRCh38 chr9: 120,980,138-120,980,519 , GRCh37.p13 chr9: 123,742,416-123,742,797 C5
    nsv6862386copy number variation1nstd229human GRCh38 chr9: 120,965,833-120,968,624 , GRCh37.p13 chr9: 123,728,111-123,730,902 C5
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6633339copy number variation1nstd224human GRCh37 chr9: 123,792,679-123,812,513 , GRCh38.p12 chr9: 121,030,401-121,050,235 C5
    nsv6573300inversion1nstd223human GRCh38 chr9: 121,072,623-121,073,705 , GRCh37.p13 chr9: 123,834,901-123,835,983 CNTRL, C5
    nsv6570581inversion1nstd223human GRCh38 chr9: 120,987,363-120,987,916 , GRCh37.p13 chr9: 123,749,641-123,750,194 C5
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