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Items: 1 to 20 of 180

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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
    nsv6895962copy number variation1nstd229human GRCh38 chr10: 118,255,301-118,303,370 , GRCh37.p13 chr10: 120,014,813-120,062,882 FAM204A
    nsv6892966copy number variation1nstd229human GRCh38 chr10: 118,285,324-118,298,176 , GRCh37.p13 chr10: 120,044,836-120,057,688 FAM204A
    nsv6892830copy number variation1nstd229human GRCh38 chr10: 117,664,803-118,402,207 , GRCh37.p13 chr10: 119,424,314-120,161,719 RAB11FIP2, FAM204A, 6 more genes
    nsv6891288copy number variation1nstd229human GRCh38 chr10: 118,300,799-118,300,980 , GRCh37.p13 chr10: 120,060,311-120,060,492 FAM204A
    nsv6889466copy number variation1nstd229human GRCh38 chr10: 118,286,023-118,298,322 , GRCh37.p13 chr10: 120,045,535-120,057,834 FAM204A
    nsv6884352copy number variation1nstd229human GRCh38 chr10: 118,290,770-118,296,908 , GRCh37.p13 chr10: 120,050,282-120,056,420 FAM204A
    nsv6884061copy number variation1nstd229human GRCh38 chr10: 118,332,525-118,332,570 , GRCh37.p13 chr10: 120,092,037-120,092,082 FAM204A
    nsv6878376copy number variation1nstd229human GRCh38 chr10: 118,321,860-118,325,319 , GRCh37.p13 chr10: 120,081,372-120,084,831 FAM204A
    nsv6878169copy number variation1nstd229human GRCh38 chr10: 118,288,919-118,296,928 , GRCh37.p13 chr10: 120,048,431-120,056,440 FAM204A
    nsv6620317copy number variation1nstd224human GRCh37 chr10: 119,424,467-120,159,880 , GRCh38.p12 chr10: 117,664,956-118,400,368 RAB11FIP2, FAM204A, 6 more genes
    nsv6455518copy number variation1nstd223human GRCh38 chr10: 118,317,964-118,318,654 , GRCh37.p13 chr10: 120,077,476-120,078,166 FAM204A
    nsv6445224copy number variation1nstd223human GRCh38 chr10: 118,320,301-118,320,857 , GRCh37.p13 chr10: 120,079,813-120,080,369 FAM204A
    nsv6439663copy number variation1nstd223human GRCh38 chr10: 118,321,860-118,325,315 , GRCh37.p13 chr10: 120,081,372-120,084,827 FAM204A
    nsv6438313copy number variation1nstd223human GRCh38 chr10: 118,285,324-118,298,173 , GRCh37.p13 chr10: 120,044,836-120,057,685 FAM204A
    nsv6437845copy number variation1nstd223human GRCh38 chr10: 118,255,301-118,303,367 , GRCh37.p13 chr10: 120,014,813-120,062,879 FAM204A
    nsv6437458copy number variation1nstd223human GRCh38 chr10: 118,316,601-118,317,600 , GRCh37.p13 chr10: 120,076,113-120,077,112 FAM204A
    nsv6314129copy number variation1nstd102humanPathogenic GRCh37 chr10: 117,019,650-125,217,066 , GRCh38.p12 chr10: 115,260,173-123,457,550 PDZD8, MIR3663HG, 122 more genes
    nsv6314085copy number variation1nstd102humanPathogenic GRCh37 chr10: 108,455,687-135,427,143 , GRCh38.p12 chr10: 106,695,929-133,613,639 LOC107984268, DPYSL4, 379 more genes
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