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Items: 1 to 20 of 503

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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
    nsv7145800insertion1nstd232human GRCh37.p13 chr10: 134,328,145-134,328,145 , GRCh38.p12 chr10: 132,514,641-132,514,641 LOC107984282
    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
    nsv6897070copy number variation1nstd229human GRCh38 chr10: 132,517,620-132,522,075 , GRCh37.p13 chr10: 134,331,124-134,335,579 LOC107984282
    nsv6895015copy number variation1nstd229human GRCh38 chr10: 132,509,380-132,515,541 , GRCh37.p13 chr10: 134,322,884-134,329,045 LOC107984282
    nsv6895003copy number variation1nstd229human GRCh38 chr10: 132,504,510-132,509,828 , GRCh37.p13 chr10: 134,318,014-134,323,332 LOC107984282
    nsv6894078copy number variation1nstd229human GRCh38 chr10: 132,522,752-132,525,098 , GRCh37.p13 chr10: 134,336,256-134,338,602 LOC107984282
    nsv6885089copy number variation1nstd229human GRCh38 chr10: 132,523,117-132,523,558 , GRCh37.p13 chr10: 134,336,621-134,337,062 LOC107984282
    nsv6882766copy number variation1nstd229human GRCh38 chr10: 132,247,003-133,073,282 , GRCh37.p13 chr10: 134,060,507-134,886,786 LOC105378572, LOC105378569, 15 more genes
    nsv6882670copy number variation1nstd229human GRCh38 chr10: 132,279,936-132,773,423 , GRCh37.p13 chr10: 134,093,440-134,586,927 PWWP2B, LINC03068, 6 more genes
    nsv6882001copy number variation1nstd229human GRCh38 chr10: 132,491,304-132,544,217 , GRCh37.p13 chr10: 134,304,808-134,357,721 LOC107984282, INPP5A
    nsv6880888copy number variation1nstd229human GRCh38 chr10: 132,508,421-132,514,485 , GRCh37.p13 chr10: 134,321,925-134,327,989 LOC107984282
    nsv6879351copy number variation1nstd229human GRCh38 chr10: 132,467,881-133,097,912 , GRCh37.p13 chr10: 134,281,385-134,911,416 ADGRA1, CFAP46, 11 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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