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Items: 1 to 20 of 134

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7068192inversion1nstd229human GRCh38 chr10: 118,910,158-125,783,778 , GRCh37.p13 chr10: 120,669,670-127,472,347 CTBP2, RPS26P39, 114 more genes
    nsv7067619inversion1nstd229human GRCh38 chr10: 119,030,818-119,030,931 , GRCh37.p13 chr10: 120,790,330-120,790,443 NANOS1
    nsv6896138copy number variation1nstd229human GRCh38 chr10: 118,899,347-119,334,149 , GRCh37.p13 chr10: 120,658,859-121,093,661 PRDX3, GRK5, 9 more genes
    nsv6884831copy number variation1nstd229human GRCh38 chr10: 118,993,701-119,031,000 , GRCh37.p13 chr10: 120,753,213-120,790,512 NANOS1
    nsv6585886inversion1nstd223human GRCh38 chr10: 118,910,158-125,783,778 , GRCh37.p13 chr10: 120,669,670-127,472,347 LOC105378520, SPADH, 114 more genes
    nsv6450643copy number variation1nstd223human GRCh38 chr10: 118,693,254-119,214,513 , GRCh37.p13 chr10: 120,452,766-120,974,025 SFXN4, DENND10, 11 more genes
    nsv6435809copy number variation1nstd223human GRCh38 chr10: 119,029,101-119,032,600 , GRCh37.p13 chr10: 120,788,613-120,792,112 EIF3A, NANOS1
    nsv6314129copy number variation1nstd102humanPathogenic GRCh37 chr10: 117,019,650-125,217,066 , GRCh38.p12 chr10: 115,260,173-123,457,550 PDZD8, MIR3663HG, 122 more genes
    nsv6314085copy number variation1nstd102humanPathogenic GRCh37 chr10: 108,455,687-135,427,143 , GRCh38.p12 chr10: 106,695,929-133,613,639 LOC107984268, DPYSL4, 379 more genes
    nsv6313945copy number variation1nstd102humanUncertain significance GRCh37 chr10: 120,782,191-123,155,522 , GRCh38.p12 chr10: 119,022,679-121,396,008 MCMBP, GRK5, 38 more genes
    nsv6290269copy number variation1nstd102humanUncertain significance GRCh37 chr10: 118,891,670-122,349,064 , GRCh38.p12 chr10: 117,132,159-120,589,552 MCMBP, PDZD8, 54 more genes
    nsv6247603mobile element insertion1nstd215human GRCh38 chr10: 119,028,654-119,028,654 , GRCh37.p13 chr10: 120,788,166-120,788,166 NANOS1
    nsv6131932copy number variation1nstd213human GRCh37 chr10: 115,960,000-125,870,001 , GRCh38.p12 chr10: 114,200,241-124,109,956 ACADSB, DMBT1, 148 more genes
    nsv6131766copy number variation1nstd213human GRCh37 chr10: 116,010,000-125,870,001 , GRCh38.p12 chr10: 114,250,241-124,109,956 ACADSB, DMBT1, 146 more genes
    nsv6112765copy number variation1nstd102humanPathogenic GRCh37 chr10: 118,247,181-135,435,319 , GRCh38.p12 chr10: 116,487,669-133,621,815 STK32C, LOC105378542, 266 more genes
    nsv6007130copy number variation1nstd212human GRCh38 chr10: 119,027,976-119,028,036 , GRCh37.p13 chr10: 120,787,488-120,787,548 NANOS1
    nsv5974801inversion1nstd209human GRCh38 chr10: 116,446,135-119,236,441 , GRCh37.p13 chr10: 118,205,647-120,995,953 EMX2, PRLHR, 48 more genes
    nsv5672603copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 119,302,758-124,813,305 , GRCh38.p12 chr10: 117,543,247-123,053,789 ACADSB, DMBT1, 84 more genes
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