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Items: 1 to 20 of 248

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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
    nsv7066100inversion1nstd229human GRCh38 chr10: 130,461,050-131,614,435 , GRCh37.p13 chr10: 132,259,314-133,446,771 LOC101927461, LOC107984186, 5 more genes
    nsv7060863inversion1nstd229human GRCh38 chr10: 127,697,992-132,467,329 , GRCh37.p13 chr10: 129,496,256-134,280,833 EBF3-AS1, GLRX3, 47 more genes
    nsv6891179copy number variation1nstd229human GRCh38 chr10: 131,049,156-131,126,885 , GRCh37.p13 chr10: 132,847,419-132,925,148 TCERG1L, LOC107984186, 1 more genes
    nsv6888543copy number variation1nstd229human GRCh38 chr10: 130,678,559-131,226,115 , GRCh37.p13 chr10: 132,476,823-133,024,378 TCERG1L, MIR378C, 4 more genes
    nsv6637925copy number variation1nstd102humanUncertain significance GRCh37 chr10: 132,844,200-132,899,703 , GRCh38.p12 chr10: 131,045,937-131,101,440 TCERG1L, TCERG1L-AS1, 1 more genes
    nsv6637882copy number variation1nstd102humanUncertain significance GRCh37 chr10: 132,631,529-135,354,972 , GRCh38.p12 chr10: 130,833,266-133,541,468 TCERG1L-AS1, PPP2R2D, 57 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
    nsv6637243copy number variation1nstd102humanPathogenic GRCh37 chr10: 130,043,370-135,345,340 , GRCh38.p12 chr10: 128,245,106-133,531,836 DPYSL4, LINC02667, 79 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
    nsv6455583copy number variation1nstd223human GRCh38 chr10: 130,983,601-131,184,500 , GRCh37.p13 chr10: 132,781,864-132,982,763 LOC107984186, TCERG1L, 1 more genes
    nsv6451700copy number variation1nstd223human GRCh38 chr10: 130,691,301-131,358,900 , GRCh37.p13 chr10: 132,489,565-133,157,163 LOC105378563, TCERG1L-AS1, 5 more genes
    nsv6450442copy number variation1nstd223human GRCh38 chr10: 131,042,201-131,592,500 , GRCh37.p13 chr10: 132,840,464-133,258,318 LOC101927461, TCERG1L, 3 more genes
    nsv6445980copy number variation1nstd223human GRCh38 chr10: 131,093,801-131,094,700 , GRCh37.p13 chr10: 132,892,064-132,892,963 TCERG1L-AS1, TCERG1L
    nsv6439552copy number variation1nstd223human GRCh38 chr10: 130,983,001-131,185,100 , GRCh37.p13 chr10: 132,781,264-132,983,363 TCERG1L-AS1, LOC107984186, 1 more genes
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