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Items: 1 to 20 of 102

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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
    nsv7098887copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,249,133-97,616,970 , GRCh38.p12 chr10: 91,489,376-95,857,213 LGI1, LOC107984257, 79 more genes
    nsv7073775inversion1nstd229human GRCh38 chr10: 92,205,149-92,554,453 , GRCh37.p13 chr10: 93,964,906-94,314,210 MARK2P9, RNY3P12, 4 more genes
    nsv6888920copy number variation1nstd229human GRCh38 chr10: 92,197,901-92,222,700 , GRCh37.p13 chr10: 93,957,658-93,982,457 NHP2P1, CPEB3
    nsv6881590copy number variation1nstd229human GRCh38 chr10: 92,214,385-92,222,050 , GRCh37.p13 chr10: 93,974,142-93,981,807 CPEB3, NHP2P1
    nsv6880995copy number variation1nstd229human GRCh38 chr10: 92,209,959-92,232,852 , GRCh37.p13 chr10: 93,969,716-93,992,609 CPEB3, NHP2P1
    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
    nsv6620929copy number variation1nstd224human GRCh37 chr10: 93,412,994-94,014,958 , GRCh38.p12 chr10: 91,653,237-92,255,201 EIF4A1P8, LOC107984253, 11 more genes
    nsv6577165inversion1nstd223human GRCh38 chr10: 92,215,773-92,217,257 , GRCh37.p13 chr10: 93,975,530-93,977,014 CPEB3, NHP2P1
    nsv6445363copy number variation1nstd223human GRCh38 chr10: 92,197,932-92,222,636 , GRCh37.p13 chr10: 93,957,689-93,982,393 NHP2P1, CPEB3
    nsv6131818copy number variation1nstd213human GRCh37 chr10: 93,940,000-94,230,001 , GRCh38.p12 chr10: 92,180,243-92,470,244 IDE, CPEB3, 4 more genes
    nsv5921993copy number variation1nstd209human GRCh38 chr10: 90,979,234-99,692,336 , GRCh37.p13 chr10: 92,738,991-101,452,093 , CYP2C115P, 166 more genes
    nsv5476085copy number variation1nstd206human GRCh38 chr10: 92,214,363-92,227,983 , GRCh37.p13 chr10: 93,974,120-93,987,740 NHP2P1, CPEB3
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4986652copy number variation1nstd200human GRCh38 chr10: 92,213,466-92,214,744 , GRCh37.p13 chr10: 93,973,223-93,974,501 NHP2P1, CPEB3
    nsv4986651copy number variation1nstd200human GRCh38 chr10: 92,197,932-92,222,635 , GRCh37.p13 chr10: 93,957,689-93,982,392 NHP2P1, CPEB3
    nsv4839110copy number variation1nstd200human GRCh37 chr10: 93,975,237-93,975,563 , GRCh38.p12 chr10: 92,215,480-92,215,806 CPEB3, NHP2P1
    nsv4835516copy number variation1nstd200human GRCh37 chr10: 93,973,223-93,974,501 , GRCh38.p12 chr10: 92,213,466-92,214,744 NHP2P1, CPEB3
    nsv4618016copy number variation1nstd183human GRCh37 chr10: 93,957,559-93,983,154 , GRCh38.p12 chr10: 92,197,802-92,223,397 NHP2P1, CPEB3
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