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Items: 1 to 20 of 230

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148117copy number variation1nstd102humanPathogenic GRCh37 chr10: 81,611,360-89,264,122 , GRCh38.p12 chr10: 79,851,604-87,504,365 ANXA11, FAM245A, 115 more genes
    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
    nsv7073059inversion1nstd229human GRCh38 chr10: 80,346,477-80,350,012 , GRCh37.p13 chr10: 82,106,233-82,109,768 DYDC1, DYDC2
    nsv7060167inversion1nstd229human GRCh38 chr10: 80,346,208-80,351,433 , GRCh37.p13 chr10: 82,105,964-82,111,189 DYDC2, DYDC1
    nsv7059604inversion1nstd229human GRCh38 chr10: 80,346,479-80,351,415 , GRCh37.p13 chr10: 82,106,235-82,111,171 DYDC2, DYDC1
    nsv6896866copy number variation1nstd229human GRCh38 chr10: 80,091,600-80,388,756 , GRCh37.p13 chr10: 81,851,356-82,148,512 LINC00857, EIF5AP4, 10 more genes
    nsv6893720copy number variation1nstd229human GRCh38 chr10: 76,896,077-84,570,412 , GRCh37.p13 chr10: 78,655,835-86,330,168 RNU6-129P, LOC105378392, 111 more genes
    nsv6890726copy number variation1nstd229human GRCh38 chr10: 80,350,354-80,354,638 , GRCh37.p13 chr10: 82,110,110-82,114,394 DYDC1, DYDC2
    nsv6887515copy number variation1nstd229human GRCh38 chr10: 80,335,027-80,357,804 , GRCh37.p13 chr10: 82,094,783-82,117,560 DYDC2, DYDC1
    nsv6886439copy number variation1nstd229human GRCh38 chr10: 80,339,560-80,344,310 , GRCh37.p13 chr10: 82,099,316-82,104,066 DYDC2, DYDC1
    nsv6881089copy number variation1nstd229human GRCh38 chr10: 80,299,965-80,973,968 , GRCh37.p13 chr10: 82,059,721-82,733,724 DYDC1, TSPAN14-AS1, 9 more genes
    nsv6620681copy number variation2nstd224human GRCh37 chr10: 82,098,248-82,112,873 , GRCh38.p12 chr10: 80,338,492-80,353,117 DYDC2, DYDC1
    nsv6620680copy number variation2nstd224human GRCh37 chr10: 82,098,248-82,112,279 , GRCh38.p12 chr10: 80,338,492-80,352,523 DYDC2, DYDC1
    nsv6620611copy number variation1nstd224human GRCh37 chr10: 82,062,661-82,112,873 , GRCh38.p12 chr10: 80,302,905-80,353,117 DYDC2, DYDC1
    nsv6620610copy number variation1nstd224human GRCh37 chr10: 82,062,661-82,102,097 , GRCh38.p12 chr10: 80,302,905-80,342,341 DYDC1
    nsv6620535copy number variation1nstd224human GRCh37 chr10: 82,049,272-82,112,873 , GRCh38.p12 chr10: 80,289,516-80,353,117 MAT1A, ZNF519P1, 2 more genes
    nsv6585055inversion1nstd223human GRCh38 chr10: 79,754,380-87,461,415 , GRCh37.p13 chr10: 81,514,136-89,221,172 DYDC2, LOC105378394, 114 more genes
    nsv6582970inversion1nstd223human GRCh38 chr10: 80,346,519-80,350,013 , GRCh37.p13 chr10: 82,106,275-82,109,769 DYDC1, DYDC2
    nsv6578729inversion1nstd223human GRCh38 chr10: 80,346,641-80,346,987 , GRCh37.p13 chr10: 82,106,397-82,106,743 DYDC1, DYDC2
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