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Items: 1 to 20 of 152

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143662insertion1nstd232human GRCh37.p13 chr10: 121,335,302-121,335,302 , GRCh38.p12 chr10: 119,575,790-119,575,790 TIAL1
    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
    nsv7076648inversion1nstd229human GRCh38 chr10: 119,076,083-120,210,505 , GRCh37.p13 chr10: 120,835,595-121,970,017 GRK5-IT1, RGS10, 23 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
    nsv6892447copy number variation1nstd229human GRCh38 chr10: 119,575,654-119,575,844 , GRCh37.p13 chr10: 121,335,166-121,335,356 TIAL1
    nsv6888711copy number variation1nstd229human GRCh38 chr10: 119,550,932-120,092,737 , GRCh37.p13 chr10: 121,310,444-121,852,249 BAG3, NACAP2, 12 more genes
    nsv6882412copy number variation1nstd229human GRCh38 chr10: 119,588,573-119,925,704 , GRCh37.p13 chr10: 121,348,085-121,685,216 RAD1P1, BAG3, 10 more genes
    nsv6637867copy number variation1nstd102humanUncertain significance GRCh37 chr10: 121,307,376-121,700,959 , GRCh38.p12 chr10: 119,547,864-119,941,447 LOC105378513, RPS8P4, 10 more genes
    nsv6594104inversion1nstd223human GRCh38 chr10: 119,572,184-119,573,064 , GRCh37.p13 chr10: 121,331,696-121,332,576 TIAL1
    nsv6585886inversion1nstd223human GRCh38 chr10: 118,910,158-125,783,778 , GRCh37.p13 chr10: 120,669,670-127,472,347 LOC105378520, SPADH, 114 more genes
    nsv6579749inversion1nstd223human GRCh38 chr10: 119,572,379-119,573,055 , GRCh37.p13 chr10: 121,331,891-121,332,567 TIAL1
    nsv6454873copy number variation1nstd223human GRCh38 chr10: 119,582,901-119,583,500 , GRCh37.p13 chr10: 121,342,413-121,343,012 TIAL1
    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
    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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