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Items: 1 to 20 of 309

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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
    nsv6895164copy number variation1nstd229human GRCh38 chr10: 114,881,333-114,881,494 , GRCh37.p13 chr10: 116,641,092-116,641,253 FHIP2A
    nsv6890100copy number variation1nstd229human GRCh38 chr10: 114,840,813-114,842,738 , GRCh37.p13 chr10: 116,600,572-116,602,497 FHIP2A
    nsv6889017copy number variation1nstd229human GRCh38 chr10: 114,270,582-115,684,161 , GRCh37.p13 chr10: 116,030,341-116,786,295 RN7SL384P, ATRNL1, 14 more genes
    nsv6885343copy number variation1nstd229human GRCh38 chr10: 114,857,435-114,859,246 , GRCh37.p13 chr10: 116,617,194-116,619,005 FHIP2A
    nsv6885301copy number variation1nstd229human GRCh38 chr10: 110,780,328-116,002,717 , GRCh37.p13 chr10: 112,540,086-116,786,295 UBE2V1P5, MIR6715A, 66 more genes
    nsv6884592copy number variation1nstd229human GRCh38 chr10: 114,898,401-114,921,200 , GRCh37.p13 chr10: 116,658,160-116,680,959 FHIP2A, RPL15P13
    nsv6884052copy number variation1nstd229human GRCh38 chr10: 114,876,531-115,123,609 , GRCh37.p13 chr10: 116,636,290-116,786,295 RNU6-1121P, RPL15P13, 6 more genes
    nsv6884019copy number variation1nstd229human GRCh38 chr10: 114,896,850-114,899,681 , GRCh37.p13 chr10: 116,656,609-116,659,440 FHIP2A, RPL15P13
    nsv6883952copy number variation1nstd229human GRCh38 chr10: 114,868,131-114,868,349 , GRCh37.p13 chr10: 116,627,890-116,628,108 FHIP2A
    nsv6881795copy number variation1nstd229human GRCh38 chr10: 114,863,438-114,892,059 , GRCh37.p13 chr10: 116,623,197-116,651,818 FHIP2A
    nsv6879415copy number variation1nstd229human GRCh38 chr10: 114,870,598-114,874,491 , GRCh37.p13 chr10: 116,630,357-116,634,250 FHIP2A
    nsv6879106copy number variation1nstd229human GRCh38 chr10: 114,853,813-114,860,768 , GRCh37.p13 chr10: 116,613,572-116,620,527 FHIP2A
    nsv6620315copy number variation1nstd224human GRCh37 chr10: 116,310,142-116,873,653 , GRCh38.p12 chr10: 114,550,383-115,113,890 ABLIM1, TRUB1, 10 more genes
    nsv6620165copy number variation1nstd224human GRCh37 chr10: 116,311,531-116,853,741 , GRCh38.p12 chr10: 114,551,772-115,093,982 ABLIM1, TRUB1, 10 more genes
    nsv6587555inversion1nstd223human GRCh38 chr10: 114,850,693-114,850,928 , GRCh37.p13 chr10: 116,610,452-116,610,687 FHIP2A
    nsv6582460inversion1nstd223human GRCh38 chr10: 114,839,214-114,839,826 , GRCh37.p13 chr10: 116,598,973-116,599,585 FHIP2A
    nsv6452361copy number variation1nstd223human GRCh38 chr10: 114,822,501-114,827,900 , GRCh37.p13 chr10: 116,582,260-116,587,659 FHIP2A
    nsv6450386copy number variation1nstd223human GRCh38 chr10: 114,817,101-114,821,600 , GRCh37.p13 chr10: 116,576,860-116,581,359 ABLIM1, FHIP2A
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