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Items: 1 to 20 of 387

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096408copy number variation1nstd102humanPathogenic GRCh37 chr2: 239,229,304-239,238,003 , GRCh38.p12 chr2: 238,320,663-238,329,362 TRAF3IP1
    nsv7096146copy number variation2nstd102humanUncertain significance GRCh37 chr2: 239,306,080-239,307,560 , GRCh38.p12 chr2: 238,397,439-238,398,919 TRAF3IP1
    nsv7093541insertion1nstd102humanUncertain significance GRCh38 chr2: 238,332,903-238,332,903 , GRCh37 chr2: 239,241,544-239,241,544 TRAF3IP1
    nsv7053948inversion1nstd229human GRCh38 chr2: 236,325,891-239,580,552 , GRCh37.p13 chr2: 237,234,534-240,502,246 PER2, MIR4269, 60 more genes
    nsv7047549inversion1nstd229human GRCh38 chr2: 236,010,287-240,118,231 , GRCh37.p13 chr2: 236,918,931-241,057,648 RAB17, COL6A3, 74 more genes
    nsv7046600inversion1nstd229human GRCh38 chr2: 237,108,675-239,672,919 , GRCh37.p13 chr2: 238,017,318-240,594,613 RBM44, MIR4440, 46 more genes
    nsv6718002copy number variation1nstd229human GRCh38 chr2: 238,041,301-238,796,100 , GRCh37.p13 chr2: 238,949,942-239,704,741 LOC105373963, SCLY, 18 more genes
    nsv6717170copy number variation1nstd229human GRCh38 chr2: 238,317,667-238,330,177 , GRCh37.p13 chr2: 239,226,308-239,238,818 TRAF3IP1
    nsv6715298copy number variation1nstd229human GRCh38 chr2: 238,326,345-238,328,527 , GRCh37.p13 chr2: 239,234,986-239,237,168 TRAF3IP1
    nsv6711510copy number variation1nstd229human GRCh38 chr2: 238,388,103-238,391,311 , GRCh37.p13 chr2: 239,296,744-239,299,952 TRAF3IP1
    nsv6709046copy number variation1nstd229human GRCh38 chr2: 238,397,633-238,402,352 , GRCh37.p13 chr2: 239,306,274-239,310,993 TRAF3IP1
    nsv6703122copy number variation1nstd229human GRCh38 chr2: 238,358,315-238,363,741 , GRCh37.p13 chr2: 239,266,956-239,272,382 TRAF3IP1
    nsv6701870copy number variation1nstd229human GRCh38 chr2: 235,899,114-238,770,175 , GRCh37.p13 chr2: 236,807,758-239,678,816 RN7SL204P, RBM44, 55 more genes
    nsv6701762copy number variation1nstd229human GRCh38 chr2: 238,337,772-238,342,037 , GRCh37.p13 chr2: 239,246,413-239,250,678 TRAF3IP1
    nsv6699181copy number variation1nstd229human GRCh38 chr2: 238,353,180-238,522,368 , GRCh37.p13 chr2: 239,261,821-239,431,009 RNU6-234P, LOC107986003, 4 more genes
    nsv6698461copy number variation1nstd229human GRCh38 chr2: 238,369,517-238,382,524 , GRCh37.p13 chr2: 239,278,158-239,291,165 TRAF3IP1
    nsv6636841copy number variation1nstd102humanPathogenic GRCh37 chr2: 236,878,509-242,783,384 , GRCh38.p12 chr2: 235,969,865-241,841,232 COPS8-DT, MTND5P46, 128 more genes
    nsv6636673copy number variation1nstd102humanPathogenic GRCh37 chr2: 235,942,616-242,783,384 , GRCh38.p12 chr2: 235,033,972-241,841,232 LINC02991, OR6B3, 136 more genes
    nsv6634398copy number variation1nstd102humanPathogenic GRCh37 chr2: 239,229,304-243,199,373 , GRCh38.p12 chr2: 238,320,663-242,157,305 HDAC4-AS1, ING5, 92 more genes
    nsv6549186inversion1nstd223human GRCh38 chr2: 238,317,195-238,319,174 , GRCh37.p13 chr2: 239,225,836-239,227,815 TRAF3IP1
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