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Items: 1 to 20 of 336

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7043684inversion1nstd229human GRCh38 chr2: 237,841,719-237,853,839 , GRCh37.p13 chr2: 238,750,362-238,762,482 RBM44
    nsv6711188copy number variation1nstd229human GRCh38 chr2: 237,829,201-238,071,700 , GRCh37.p13 chr2: 238,737,844-238,980,341 LOC105373960, SCLY, 5 more genes
    nsv6710666copy number variation1nstd229human GRCh38 chr2: 237,822,201-237,828,100 , GRCh37.p13 chr2: 238,730,844-238,736,743 RBM44
    nsv6710615copy number variation1nstd229human GRCh38 chr2: 237,778,462-237,848,128 , GRCh37.p13 chr2: 238,687,105-238,756,771 RBM44, LRRFIP1
    nsv6707514copy number variation1nstd229human GRCh38 chr2: 237,808,974-237,812,839 , GRCh37.p13 chr2: 238,717,617-238,721,482 RBM44
    nsv6704885copy number variation1nstd229human GRCh38 chr2: 237,829,088-237,829,258 , GRCh37.p13 chr2: 238,737,731-238,737,901 RBM44
    nsv6702652copy number variation1nstd229human GRCh38 chr2: 237,803,801-237,867,000 , GRCh37.p13 chr2: 238,712,444-238,775,643 RAMP1, RBM44
    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
    nsv6699735copy number variation1nstd229human GRCh38 chr2: 237,806,398-238,044,528 , GRCh37.p13 chr2: 238,715,041-238,953,169 UBE2F-SCLY, RBM44, 4 more genes
    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
    nsv6627570copy number variation1nstd224human GRCh37 chr2: 238,722,295-238,742,929 , GRCh38.p12 chr2: 237,813,652-237,834,286 RBM44
    nsv6354671copy number variation1nstd223human GRCh38 chr2: 237,818,601-237,820,200 , GRCh37.p13 chr2: 238,727,244-238,728,843 RBM44
    nsv6351471copy number variation1nstd223human GRCh38 chr2: 237,836,898-237,866,996 , GRCh37.p13 chr2: 238,745,541-238,775,639 RAMP1, RBM44
    nsv6351341copy number variation1nstd223human GRCh38 chr2: 237,802,089-237,804,089 , GRCh37.p13 chr2: 238,710,732-238,712,732 RBM44
    nsv6351012copy number variation1nstd223human GRCh38 chr2: 237,814,101-237,814,800 , GRCh37.p13 chr2: 238,722,744-238,723,443 RBM44
    nsv6346878copy number variation1nstd223human GRCh38 chr2: 237,803,795-237,843,029 , GRCh37.p13 chr2: 238,712,438-238,751,672 RBM44
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