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Items: 1 to 20 of 151

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7078018inversion1nstd229human GRCh38 chr9: 117,593,362-117,829,644 , GRCh37.p13 chr9: 120,355,640-120,591,922 LOC105376244, RNU6-1082P, 3 more genes
    nsv6872378copy number variation1nstd229human GRCh38 chr9: 116,987,526-119,256,739 , GRCh37.p13 chr9: 119,749,805-122,019,017 LOC101928849, LOC105376249, 21 more genes
    nsv6865695copy number variation1nstd229human GRCh38 chr9: 117,639,167-119,255,557 , GRCh37.p13 chr9: 120,401,445-122,017,835 LOC107987035, RPL35AP22, 14 more genes
    nsv6863757copy number variation1nstd229human GRCh38 chr9: 117,203,660-117,702,689 , GRCh37.p13 chr9: 119,965,939-120,464,967 LOC101928797, TLR4, 5 more genes
    nsv6862644copy number variation1nstd229human GRCh38 chr9: 117,724,801-117,797,500 , GRCh37.p13 chr9: 120,487,079-120,559,778 LOC105376244, TLR4
    nsv6860444copy number variation1nstd229human GRCh38 chr9: 117,656,969-117,742,626 , GRCh37.p13 chr9: 120,419,247-120,504,904 LOC101928797, TLR4, 2 more genes
    nsv6859098copy number variation1nstd229human GRCh38 chr9: 117,447,115-117,840,463 , GRCh37.p13 chr9: 120,209,393-120,602,741 LOC105376244, RNU6-1082P, 4 more genes
    nsv6637266copy number variation1nstd102humanUncertain significance GRCh37 chr9: 120,197,413-120,521,544 , GRCh38.p12 chr9: 117,435,135-117,759,266 RPL35AP22, LOC105376244, 4 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6454639copy number variation1nstd223human GRCh38 chr9: 117,708,868-117,709,361 , GRCh37.p13 chr9: 120,471,146-120,471,639 TLR4
    nsv6438569copy number variation1nstd223human GRCh38 chr9: 117,433,585-117,758,794 , GRCh37.p13 chr9: 120,195,863-120,521,072 RPL35AP22, LOC105376242, 4 more genes
    nsv6314063copy number variation1nstd102humanUncertain significance GRCh37 chr9: 119,722,551-121,219,732 , GRCh38.p12 chr9: 116,960,272-118,457,454 LOC101928797, LOC105376237, 14 more genes
    nsv6314001copy number variation1nstd102humanPathogenic GRCh37 chr9: 116,422,275-131,713,233 , GRCh38.p12 chr9: 113,659,995-128,950,954 LOC105376244, RN7SL187P, 286 more genes
    nsv6313900copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 71,349,994-122,603,410 , GRCh38.p12 chr9: 68,735,078-119,841,132 ABCA1, ALAD, 793 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6291398copy number variation1nstd102humanPathogenic GRCh37 chr9: 120,045,175-127,335,905 , GRCh38.p12 chr9: 117,282,896-124,573,626 ZBTB6, LOC105376253, 107 more genes
    nsv6290238copy number variation1nstd102humanUncertain significance GRCh37 chr9: 117,853,848-124,633,077 , GRCh38.p12 chr9: 115,091,569-121,870,798 LINC00474, LOC107987123, 72 more genes
    nsv6137438copy number variation1nstd213human GRCh37 chr9: 120,020,000-121,220,001 , GRCh38.p12 chr9: 117,257,721-118,457,723 TLR4, ASTN2, 11 more genes
    nsv6136812copy number variation1nstd213human GRCh37 chr9: 120,430,000-120,580,001 , GRCh38.p12 chr9: 117,667,722-117,817,723 TLR4, RPL35AP22, 2 more genes
    nsv5915736copy number variation1nstd209human GRCh38 chr9: 117,707,882-117,707,964 , GRCh37.p13 chr9: 120,470,160-120,470,242 RNU6-1082P, TLR4
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