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Items: 1 to 20 of 146

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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
    nsv7140445insertion1nstd232human GRCh37.p13 chr10: 124,917,399-124,917,399 , GRCh38.p12 chr10: 123,157,883-123,157,883 BUB3
    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
    nsv6892577copy number variation1nstd229human GRCh38 chr10: 121,685,649-124,297,191 , GRCh37.p13 chr10: 123,445,163-125,985,760 LOC107984128, ATE1-AS1, 39 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
    nsv6881838copy number variation1nstd229human GRCh38 chr10: 123,143,703-123,188,583 , GRCh37.p13 chr10: 124,903,219-124,948,099 RPS26P39, BUB3, 2 more genes
    nsv6638052copy number variation1nstd102humanUncertain significance GRCh37 chr10: 124,252,660-125,447,562 , GRCh38.p12 chr10: 122,493,144-123,688,046 C10orf88B, IKZF5, 20 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
    nsv6452172copy number variation1nstd223human GRCh38 chr10: 123,089,191-123,449,664 , GRCh37.p13 chr10: 124,848,707-125,209,180 HMX2, RPS26P39, 4 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
    nsv6308448mobile element insertion1nstd186human GRCh37 chr10: 124,923,698-124,923,749 , GRCh38.p12 chr10: 123,164,182-123,164,233 BUB3
    nsv6131939copy number variation1nstd213human GRCh37 chr10: 124,920,000-125,080,001 , GRCh38.p12 chr10: 123,160,484-123,320,485 BUB3, RPS26P39, 1 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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