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Items: 1 to 20 of 113

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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
    nsv7074263inversion1nstd229human GRCh38 chr10: 118,757,649-119,005,677 , GRCh37.p13 chr10: 120,517,161-120,765,189 RPL17P36, LDHAP5, 1 more genes
    nsv7073963inversion1nstd229human GRCh38 chr10: 118,931,145-118,933,656 , GRCh37.p13 chr10: 120,690,657-120,693,168 LDHAP5
    nsv7068192inversion1nstd229human GRCh38 chr10: 118,910,158-125,783,778 , GRCh37.p13 chr10: 120,669,670-127,472,347 CTBP2, RPS26P39, 114 more genes
    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
    nsv6895946copy number variation1nstd229human GRCh38 chr10: 118,931,280-118,935,070 , GRCh37.p13 chr10: 120,690,792-120,694,582 LDHAP5
    nsv6887319copy number variation1nstd229human GRCh38 chr10: 118,901,215-118,970,909 , GRCh37.p13 chr10: 120,660,727-120,730,421 LDHAP5
    nsv6881312copy number variation1nstd229human GRCh38 chr10: 118,918,285-118,954,507 , GRCh37.p13 chr10: 120,677,797-120,714,019 LDHAP5
    nsv6878590copy number variation1nstd229human GRCh38 chr10: 118,914,728-118,962,899 , GRCh37.p13 chr10: 120,674,240-120,722,411 LDHAP5
    nsv6585886inversion1nstd223human GRCh38 chr10: 118,910,158-125,783,778 , GRCh37.p13 chr10: 120,669,670-127,472,347 LOC105378520, SPADH, 114 more genes
    nsv6454065copy number variation1nstd223human GRCh38 chr10: 118,931,280-118,935,070 , GRCh37.p13 chr10: 120,690,792-120,694,582 LDHAP5
    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
    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
    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
    nsv6131937copy number variation1nstd213human GRCh37 chr10: 119,240,000-120,730,001 , GRCh38.p12 chr10: 117,480,489-118,970,489 EMX2, PRLHR, 16 more genes
    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
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