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Items: 1 to 20 of 168

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148086copy number variation1nstd102humanPathogenic GRCh37 chr10: 124,895,517-135,440,296 , GRCh38.p12 chr10: 123,136,001-133,626,792 FANK1, LOC105378534, 159 more genes
    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
    nsv7137208copy number variation1nstd102humanPathogenic GRCh37 chr10: 123,477,898-135,427,143 , GRCh38.p12 chr10: 121,718,384-133,613,639 ZRANB1, LOC105378544, 182 more genes
    nsv7098893copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,610,933-135,439,810 , GRCh38.p12 chr10: 120,851,421-133,626,306 LOC105378571, DOCK1, 196 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
    nsv7061393inversion1nstd229human GRCh38 chr10: 125,582,588-126,853,126 , GRCh37.p13 chr10: 127,271,157-128,541,695 RNA5SP328, ADAM12, 23 more genes
    nsv6889377copy number variation1nstd229human GRCh38 chr10: 125,039,754-126,334,234 , GRCh37.p13 chr10: 126,728,323-128,022,803 LOC102724793, LOC105378541, 26 more genes
    nsv6884703copy number variation1nstd229human GRCh38 chr10: 121,934,615-128,427,106 , GRCh37.p13 chr10: 123,694,130-130,225,370 OAT, C10orf88, 98 more genes
    nsv6637456copy number variation1nstd102humanUncertain significance GRCh37 chr10: 126,662,496-133,985,966 , GRCh38.p12 chr10: 124,973,927-132,172,462 LOC107984186, LOC105378550, 82 more genes
    nsv6634415copy number variation1nstd102humanPathogenic GRCh37 chr10: 126,914,469-135,427,143 , GRCh38.p12 chr10: 125,225,900-133,613,639 MGMT, LINC01168, 127 more genes
    nsv6634408copy number variation1nstd102humanPathogenic GRCh37 chr10: 127,198,625-135,427,143 , GRCh38.p12 chr10: 125,510,056-133,613,639 MIR202HG, LOC105378563, 123 more genes
    nsv6585886inversion1nstd223human GRCh38 chr10: 118,910,158-125,783,778 , GRCh37.p13 chr10: 120,669,670-127,472,347 LOC105378520, SPADH, 114 more genes
    nsv6436096copy number variation1nstd223human GRCh38 chr10: 125,663,485-125,664,945 , GRCh37.p13 chr10: 127,352,054-127,353,514 TEX36, ALDOAP2
    nsv6315265copy number variation1nstd102humanUncertain significance GRCh38 chr10: 124,920,875-125,841,697 , GRCh37.p13 chr10: 126,609,444-127,530,266 TEX36-AS1, LOC105378542, 21 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
    nsv6291412copy number variation1nstd102humanUncertain significance GRCh37 chr10: 127,128,172-127,999,424 , GRCh38.p12 chr10: 125,439,603-126,310,855 RNU2-42P, LOC105378544, 22 more genes
    nsv6131940copy number variation2nstd213human GRCh37 chr10: 125,920,000-128,610,001 , GRCh38.p12 chr10: 124,231,431-126,921,432 ALDOAP2, CTBP2, 47 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
    nsv5980446copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,785,023-135,457,222 , GRCh38.p12 chr10: 121,025,510-133,643,718 LINC02641, CFAP46, 194 more genes
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