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Items: 1 to 20 of 205

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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
    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
    nsv7093624copy number variation1nstd102humanUncertain significance GRCh37 chr10: 124,214,244-124,273,875 , GRCh38.p12 chr10: 122,454,728-122,514,359 LOC105378525, HTRA1, 1 more genes
    nsv7093623copy number variation1nstd102humanUncertain significance GRCh37 chr10: 123,239,371-124,813,281 , GRCh38.p12 chr10: 121,479,857-123,053,765 TACC2, BTBD16, 25 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
    nsv6890687copy number variation1nstd229human GRCh38 chr10: 122,457,323-122,457,747 , GRCh37.p13 chr10: 124,216,839-124,217,263 LOC105378525, ARMS2
    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
    nsv6879728copy number variation1nstd229human GRCh38 chr10: 122,447,895-122,453,423 , GRCh37.p13 chr10: 124,207,411-124,212,939 LOC105378525, ARMS2
    nsv6637491copy number variation1nstd102humanUncertain significance GRCh37 chr10: 123,964,214-124,477,580 , GRCh38.p12 chr10: 122,204,699-122,718,064 TACC2, PLEKHA1, 9 more genes
    nsv6586169inversion1nstd223human GRCh38 chr10: 122,453,211-122,453,792 , GRCh37.p13 chr10: 124,212,727-124,213,308 ARMS2, LOC105378525
    nsv6585886inversion1nstd223human GRCh38 chr10: 118,910,158-125,783,778 , GRCh37.p13 chr10: 120,669,670-127,472,347 LOC105378520, SPADH, 114 more genes
    nsv6449809copy number variation1nstd223human GRCh38 chr10: 122,457,323-122,457,747 , GRCh37.p13 chr10: 124,216,839-124,217,263 LOC105378525, ARMS2
    nsv6315094delins1nstd102humanrisk factor GRCh37 chr10: 124,216,821-124,217,264 , GRCh38 chr10: 122,457,305-122,457,748 ARMS2, LOC105378525
    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
    nsv6132024copy number variation1nstd213human GRCh37 chr10: 124,170,000-124,380,001 , GRCh38.p12 chr10: 122,410,484-122,620,485 DMBT1, HTRA1, 4 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
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