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Items: 1 to 20 of 948

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095100copy number variation1nstd102humanPathogenic GRCh37 chr16: 78,133,676-79,633,799 , GRCh38.p12 chr16: 78,099,779-79,599,902 RPS3P7, RNA5SP431, 8 more genes
    nsv7076891inversion1nstd229human GRCh38 chr16: 79,588,144-79,590,717 , GRCh37.p13 chr16: 79,622,041-79,624,614 MAF
    nsv7075974inversion1nstd229human GRCh38 chr16: 79,467,043-79,479,311 , GRCh37.p13 chr16: 79,500,940-79,513,208 MAF
    nsv7070802inversion1nstd229human GRCh38 chr16: 79,191,746-79,200,888 , GRCh37.p13 chr16: 79,225,643-79,234,785 MAF, WWOX
    nsv7069467inversion1nstd229human GRCh38 chr16: 77,603,047-81,438,175 , GRCh37.p13 chr16: 77,636,944-81,471,780 ATMIN, WWOX, 39 more genes
    nsv7066884inversion1nstd229human GRCh38 chr16: 79,588,009-79,592,818 , GRCh37.p13 chr16: 79,621,906-79,626,715 MAF
    nsv7062267inversion1nstd229human GRCh38 chr16: 79,449,960-79,454,640 , GRCh37.p13 chr16: 79,483,857-79,488,537 MAF
    nsv6997645copy number variation1nstd229human GRCh38 chr16: 79,288,075-79,292,094 , GRCh37.p13 chr16: 79,321,972-79,325,991 MAF
    nsv6997534copy number variation1nstd229human GRCh38 chr16: 79,568,704-79,593,530 , GRCh37.p13 chr16: 79,602,601-79,627,427 MAF
    nsv6997192copy number variation1nstd229human GRCh38 chr16: 79,433,161-79,440,349 , GRCh37.p13 chr16: 79,467,058-79,474,246 MAF
    nsv6996557copy number variation1nstd229human GRCh38 chr16: 79,359,683-79,364,956 , GRCh37.p13 chr16: 79,393,580-79,398,853 MAF
    nsv6996445copy number variation1nstd229human GRCh38 chr16: 79,414,073-79,417,952 , GRCh37.p13 chr16: 79,447,970-79,451,849 MAF
    nsv6996183copy number variation1nstd229human GRCh38 chr16: 79,436,238-79,459,701 , GRCh37.p13 chr16: 79,470,135-79,493,598 MAF
    nsv6995658copy number variation1nstd229human GRCh38 chr16: 79,240,499-79,240,527 , GRCh37.p13 chr16: 79,274,396-79,274,424 MAF
    nsv6995578copy number variation1nstd229human GRCh38 chr16: 79,319,751-79,321,882 , GRCh37.p13 chr16: 79,353,648-79,355,779 MAF
    nsv6995353copy number variation1nstd229human GRCh38 chr16: 79,466,139-79,475,974 , GRCh37.p13 chr16: 79,500,036-79,509,871 MAF
    nsv6994835copy number variation1nstd229human GRCh38 chr16: 78,796,234-79,431,180 , GRCh37.p13 chr16: 78,830,131-79,465,077 RNA5SP431, MAF, 4 more genes
    nsv6994608copy number variation1nstd229human GRCh38 chr16: 76,392,054-84,158,971 , GRCh37.p13 chr16: 76,425,951-84,192,576 , MAFTRR, 87 more genes
    nsv6994410copy number variation1nstd229human GRCh38 chr16: 79,127,299-79,282,116 , GRCh37.p13 chr16: 79,161,196-79,316,013 MAF, RNA5SP431, 1 more genes
    nsv6994379copy number variation1nstd229human GRCh38 chr16: 79,221,301-79,249,100 , GRCh37.p13 chr16: 79,255,198-79,282,997 MAF
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