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Items: 1 to 20 of 99

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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
    nsv7073007inversion1nstd229human GRCh38 chr10: 83,678,437-92,070,274 , GRCh37.p13 chr10: 85,438,193-93,830,031 PPP1R3C, LOC105378415, 157 more genes
    nsv7065381inversion1nstd229human GRCh38 chr10: 83,674,811-92,070,275 , GRCh37.p13 chr10: 85,434,567-93,830,032 LINC01520, RPS27P1, 158 more genes
    nsv6637868copy number variation1nstd102humanPathogenic GRCh37 chr10: 89,823,147-96,056,941 , GRCh38.p12 chr10: 88,063,390-94,297,184 RPS27P1, RNLS, 118 more genes
    nsv6637542copy number variation1nstd102humanPathogenic GRCh37 chr10: 82,595,472-93,542,416 , GRCh38.p12 chr10: 80,835,716-91,782,659 IFIT6P, HECTD2, 166 more genes
    nsv6634458copy number variation1nstd102humanPathogenic GRCh37 chr10: 83,533,660-91,913,077 , GRCh38.p12 chr10: 81,773,904-90,153,320 IFIT5, IFIT1, 140 more genes
    nsv6451406copy number variation1nstd223human GRCh38 chr10: 89,687,601-89,690,300 , GRCh37.p13 chr10: 91,447,358-91,450,057 FLJ37201
    nsv6436412copy number variation1nstd223human GRCh38 chr10: 89,692,601-89,695,000 , GRCh37.p13 chr10: 91,452,358-91,454,757 FLJ37201
    nsv6292773mobile element insertion1nstd186human GRCh37 chr10: 91,451,843-91,451,894 , GRCh38.p12 chr10: 89,692,086-89,692,137 FLJ37201
    nsv5710814mobile element insertion1nstd211human GRCh38 chr10: 89,692,086-89,692,086 , GRCh37.p13 chr10: 91,451,843-91,451,843 FLJ37201
    nsv5398677mobile element insertion1nstd206human GRCh38 chr10: 89,692,086-89,692,137 , GRCh37.p13 chr10: 91,451,843-91,451,894 FLJ37201
    nsv5347970translocation1nstd200human GRCh38 chr10: 89,694,193-89,694,193 , GRCh38 chr10: 89,694,141-89,694,141 , GRCh37.p13 chr10: 91,453,950-91,453,950 , GRCh37.p13 chr10: 91,453,898-91,453,898 FLJ37201
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4986573copy number variation1nstd200human GRCh38 chr10: 89,687,636-89,689,757 , GRCh37.p13 chr10: 91,447,393-91,449,514 FLJ37201
    nsv4986572copy number variation1nstd200human GRCh38 chr10: 89,674,272-89,791,874 , GRCh37.p13 chr10: 91,434,029-91,551,631 KIF20B, MTND5P42, 1 more genes
    nsv4973879copy number variation1nstd200human GRCh38 chr10: 89,689,773-89,689,961 , GRCh37.p13 chr10: 91,449,530-91,449,718 FLJ37201
    nsv4973877copy number variation1nstd200human GRCh38 chr10: 89,366,953-89,877,440 , GRCh37.p13 chr10: 91,126,710-91,637,197 SLC16A12-AS1, LINC00865, 14 more genes
    nsv4836481copy number variation1nstd200human GRCh37 chr10: 91,449,530-91,449,718 , GRCh38.p12 chr10: 89,689,773-89,689,961 FLJ37201
    nsv4833445copy number variation1nstd200human GRCh37 chr10: 91,126,710-91,637,197 , GRCh38.p12 chr10: 89,366,953-89,877,440 SLC16A12, PANK1, 14 more genes
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