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Items: 1 to 20 of 128

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6812046copy number variation1nstd229human GRCh38 chr6: 96,887,904-96,891,737 , GRCh37.p13 chr6: 97,335,780-97,339,613 NDUFAF4
    nsv6807010copy number variation1nstd229human GRCh38 chr6: 96,887,534-96,887,838 , GRCh37.p13 chr6: 97,335,410-97,335,714 NDUFAF4
    nsv6804328copy number variation1nstd229human GRCh38 chr6: 96,897,922-96,916,301 , GRCh37.p13 chr6: 97,345,798-97,364,177 RN7SL509P, NDUFAF4, 1 more genes
    nsv6636533copy number variation1nstd102humanPathogenic GRCh37 chr6: 96,596,732-105,554,568 , GRCh38.p12 chr6: 96,148,856-105,106,693 MCHR2-AS1, ACTG1P18, 65 more genes
    nsv6636338copy number variation1nstd102humanPathogenic GRCh37 chr6: 96,946,110-106,497,526 , GRCh38.p12 chr6: 96,498,234-106,049,651 BVES-AS1, LIN28B, 74 more genes
    nsv6634392copy number variation1nstd102humanUncertain significance GRCh37 chr6: 78,911,022-98,909,173 , GRCh38.p12 chr6: 78,201,305-98,461,297 MTHFD2P2, RPL7P27, 212 more genes
    nsv6631277copy number variation1nstd224human GRCh37 chr6: 95,390,186-97,681,784 , GRCh38.p12 chr6: 94,680,468-97,233,908 NDUFAF4, MANEA, 21 more genes
    nsv6612338copy number variation1nstd223human GRCh38 chr6: 96,887,532-96,887,838 , GRCh37.p13 chr6: 97,335,408-97,335,714 NDUFAF4
    nsv6602081copy number variation1nstd223human GRCh38 chr6: 96,894,201-96,904,500 , GRCh37.p13 chr6: 97,342,077-97,352,376 NDUFAF4, KLHL32
    nsv6313858copy number variation1nstd102humanPathogenic GRCh37 chr6: 92,054,891-118,329,651 , GRCh38.p12 chr6: 91,345,173-118,008,488 RN7SL509P, LAMA4, 311 more genes
    nsv6312510copy number variation1nstd102humanUncertain significance GRCh37 chr6: 97,338,980-97,339,287 , GRCh38.p12 chr6: 96,891,104-96,891,411 NDUFAF4
    nsv6312412copy number variation1nstd102humanUncertain significance GRCh37 chr6: 97,338,980-97,345,677 , GRCh38.p12 chr6: 96,891,104-96,897,801 NDUFAF4, KLHL32
    nsv6291344copy number variation1nstd102humanUncertain significance GRCh37 chr6: 97,115,084-97,372,081 , GRCh38.p12 chr6: 96,667,208-96,924,205 EEF1GP6, GPR63, 5 more genes
    nsv5891396copy number variation1nstd209human GRCh38 chr6: 96,887,902-96,891,733 , GRCh37.p13 chr6: 97,335,778-97,339,609 NDUFAF4
    nsv5845856copy number variation1nstd209human GRCh38 chr6: 96,887,895-96,891,484 , GRCh37.p13 chr6: 97,335,771-97,339,360 NDUFAF4
    nsv5463068copy number variation1nstd206human GRCh38 chr6: 96,887,534-96,887,838 , GRCh37.p13 chr6: 97,335,410-97,335,714 NDUFAF4
    nsv5369499translocation1nstd200human GRCh38 chr6: 96,887,534-96,887,534 , GRCh38 chr6: 96,887,838-96,887,838 , GRCh37.p13 chr6: 97,335,410-97,335,410 , GRCh37.p13 chr6: 97,335,714-97,335,714 NDUFAF4
    nsv5363259translocation1nstd200human GRCh38 chr6: 156,271,318-156,271,318 , GRCh38 chr6: 96,897,885-96,897,885 , GRCh37.p13 chr6: 97,345,761-97,345,761 , GRCh37.p13 chr6: 156,592,452-156,592,452 NDUFAF4, KLHL32, 1 more genes
    nsv5363258translocation1nstd200human GRCh38 chr6: 96,889,311-96,889,311 , GRCh38 chr6: 156,271,304-156,271,304 , GRCh37.p13 chr6: 97,337,187-97,337,187 , GRCh37.p13 chr6: 156,592,438-156,592,438 LOC101928923, NDUFAF4
    nsv5330997translocation1nstd200human GRCh37 chr6: 97,335,714-97,335,714 , GRCh37 chr6: 97,335,410-97,335,410 , GRCh38.p12 chr6: 96,887,838-96,887,838 , GRCh38.p12 chr6: 96,887,534-96,887,534 NDUFAF4

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