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Items: 1 to 20 of 402

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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
    nsv7093904copy number variation1nstd102humanUncertain significance GRCh37 chr10: 99,344,461-105,992,004 , GRCh38.p12 chr10: 97,584,704-104,232,246 ABCC2, LBX1-AS1, 160 more genes
    nsv7069211inversion1nstd229human GRCh38 chr10: 97,867,662-97,867,768 , GRCh37.p13 chr10: 99,627,419-99,627,525 CRTAC1, GOLGA7B
    nsv7059886inversion1nstd229human GRCh38 chr10: 95,520,399-102,687,169 , GRCh37.p13 chr10: 97,280,156-104,446,926 , ENTPD1-AS1, 168 more genes
    nsv6897751copy number variation1nstd229human GRCh38 chr10: 98,016,934-98,021,554 , GRCh37.p13 chr10: 99,776,691-99,781,311 CRTAC1
    nsv6897724copy number variation1nstd229human GRCh38 chr10: 97,919,554-97,923,213 , GRCh37.p13 chr10: 99,679,311-99,682,970 CRTAC1
    nsv6897038copy number variation1nstd229human GRCh38 chr10: 98,029,502-98,029,530 , GRCh37.p13 chr10: 99,789,259-99,789,287 CRTAC1
    nsv6896098copy number variation1nstd229human GRCh38 chr10: 97,689,118-97,876,870 , GRCh37.p13 chr10: 99,448,875-99,636,627 CRTAC1, MARVELD1, 6 more genes
    nsv6896009copy number variation1nstd229human GRCh38 chr10: 97,916,587-97,936,367 , GRCh37.p13 chr10: 99,676,344-99,696,124 CRTAC1
    nsv6890510copy number variation1nstd229human GRCh38 chr10: 97,946,653-97,948,383 , GRCh37.p13 chr10: 99,706,410-99,708,140 CRTAC1
    nsv6890264copy number variation1nstd229human GRCh38 chr10: 97,774,186-98,040,932 , GRCh37.p13 chr10: 99,533,943-99,800,689 CRTAC1, MIR3085, 3 more genes
    nsv6890025copy number variation1nstd229human GRCh38 chr10: 97,916,636-97,919,708 , GRCh37.p13 chr10: 99,676,393-99,679,465 CRTAC1
    nsv6889750copy number variation1nstd229human GRCh38 chr10: 97,987,020-97,991,370 , GRCh37.p13 chr10: 99,746,777-99,751,127 CRTAC1
    nsv6888565copy number variation1nstd229human GRCh38 chr10: 97,943,233-97,943,484 , GRCh37.p13 chr10: 99,702,990-99,703,241 CRTAC1
    nsv6887874copy number variation1nstd229human GRCh38 chr10: 97,930,401-97,933,600 , GRCh37.p13 chr10: 99,690,158-99,693,357 CRTAC1
    nsv6885547copy number variation1nstd229human GRCh38 chr10: 97,958,537-97,961,537 , GRCh37.p13 chr10: 99,718,294-99,721,294 CRTAC1
    nsv6885311copy number variation1nstd229human GRCh38 chr10: 97,924,540-97,931,756 , GRCh37.p13 chr10: 99,684,297-99,691,513 CRTAC1
    nsv6885141copy number variation1nstd229human GRCh38 chr10: 97,985,953-97,988,533 , GRCh37.p13 chr10: 99,745,710-99,748,290 CRTAC1
    nsv6884956copy number variation1nstd229human GRCh38 chr10: 97,872,483-97,876,775 , GRCh37.p13 chr10: 99,632,240-99,636,532 CRTAC1, MIR3085
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