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Items: 1 to 20 of 462

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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
    nsv7072964inversion1nstd229human GRCh38 chr10: 133,231,135-133,235,978 , GRCh37.p13 chr10: 135,044,639-135,049,482 VENTX, UTF1
    nsv7061137inversion1nstd229human GRCh38 chr10: 132,930,727-133,231,794 , GRCh37.p13 chr10: 134,744,231-135,045,298 KNDC1, LOC112268067, 12 more genes
    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
    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
    nsv6890181copy number variation1nstd229human GRCh38 chr10: 133,179,701-133,283,600 , GRCh37.p13 chr10: 134,993,205-135,097,104 MIR202HG, MIR202, 7 more genes
    nsv6888535copy number variation1nstd229human GRCh38 chr10: 133,227,205-133,231,843 , GRCh37.p13 chr10: 135,040,709-135,045,347 UTF1
    nsv6886023copy number variation1nstd229human GRCh38 chr10: 133,130,095-133,254,344 , GRCh37.p13 chr10: 134,943,599-135,067,848 ADGRA1, MIR202HG, 7 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
    nsv6637940copy number variation1nstd102humanUncertain significance GRCh37 chr10: 134,589,740-135,125,943 , GRCh38.p12 chr10: 132,776,236-133,312,439 INPP5A, LOC107984283, 21 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
    nsv6443934copy number variation1nstd223human GRCh38 chr10: 132,987,480-133,379,817 , GRCh37.p13 chr10: 134,800,984-135,193,321 BANF1P2, ADAM8, 20 more genes
    nsv6315498copy number variation1nstd102humanPathogenic GRCh37 chr10: 129,605,105-135,427,143 , GRCh38.p12 chr10: 127,806,841-133,613,639 LINC02646, GLRX3, 87 more genes
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