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Items: 1 to 20 of 432

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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
    nsv7072859inversion1nstd229human GRCh38 chr10: 133,385,648-133,393,197 , GRCh37.p13 chr10: 135,199,152-135,206,701 PAOX, MTG1
    nsv7065982inversion1nstd229human GRCh38 chr10: 133,381,581-133,388,320 , GRCh37.p13 chr10: 135,195,085-135,201,824 PAOX
    nsv6897201copy number variation1nstd229human GRCh38 chr10: 133,055,806-133,380,114 , GRCh37.p13 chr10: 134,869,310-135,193,618 ECHS1, MIR202, 18 more genes
    nsv6894124copy number variation1nstd229human GRCh38 chr10: 133,383,725-133,438,234 , GRCh37.p13 chr10: 135,197,229-135,251,738 PAOX, OR6L2P, 2 more genes
    nsv6893113copy number variation1nstd229human GRCh38 chr10: 133,214,920-133,404,255 , GRCh37.p13 chr10: 135,028,424-135,217,759 FUOM, VENTX, 15 more genes
    nsv6892371copy number variation1nstd229human GRCh38 chr10: 133,346,604-133,601,246 , GRCh37.p13 chr10: 135,160,108-135,414,750 PRAP1, MIR3944, 13 more genes
    nsv6891689copy number variation1nstd229human GRCh38 chr10: 133,252,351-133,481,239 , GRCh37.p13 chr10: 135,065,855-135,294,743 MTG1, OR6L2P, 13 more genes
    nsv6890950copy number variation1nstd229human GRCh38 chr10: 133,249,603-133,455,749 , GRCh37.p13 chr10: 135,063,107-135,269,253 SCART1, FUOM, 12 more genes
    nsv6890579copy number variation1nstd229human GRCh38 chr10: 133,379,559-133,384,953 , GRCh37.p13 chr10: 135,193,063-135,198,457 PAOX
    nsv6890331copy number variation1nstd229human GRCh38 chr10: 133,240,824-133,449,715 , GRCh37.p13 chr10: 135,054,328-135,263,219 MTG1, VENTX, 14 more genes
    nsv6882299copy number variation1nstd229human GRCh38 chr10: 132,961,268-133,490,334 , GRCh37.p13 chr10: 134,774,772-135,303,838 LOC107984283, PRAP1, 29 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
    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
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