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Items: 1 to 20 of 844

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6129441insertion1nstd186human GRCh37 chr18: 24,538,013-24,538,013 , GRCh38.p12 chr18: 26,958,049-26,958,049 CHST9
    nsv6128401copy number variation1nstd186human GRCh37 chr18: 24,555,665-24,557,024 , GRCh38.p12 chr18: 26,975,701-26,977,060 CHST9
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv5970700insertion1nstd209human GRCh38 chr18: 26,958,049-26,958,049 , GRCh37.p13 chr18: 24,538,013-24,538,013 CHST9
    nsv5947298copy number variation1nstd209human GRCh38 chr18: 26,937,083-26,937,134 , GRCh37.p13 chr18: 24,517,047-24,517,098 CHST9
    nsv5946801copy number variation1nstd209human GRCh38 chr18: 26,975,698-26,977,059 , GRCh37.p13 chr18: 24,555,662-24,557,023 CHST9
    nsv5944605copy number variation1nstd209human GRCh38 chr18: 27,128,298-27,129,405 , GRCh37.p13 chr18: 24,708,262-24,709,369 CHST9
    nsv5941088copy number variation1nstd209human GRCh38 chr18: 27,097,430-27,101,079 , GRCh37.p13 chr18: 24,677,394-24,681,043 CHST9
    nsv5938802copy number variation1nstd209human GRCh38 chr18: 27,044,291-27,044,573 , GRCh37.p13 chr18: 24,624,255-24,624,537 CHST9
    nsv5937504copy number variation1nstd209human GRCh38 chr18: 26,996,556-27,000,742 , GRCh37.p13 chr18: 24,576,520-24,580,706 CHST9
    nsv5937490copy number variation1nstd209human GRCh38 chr18: 26,991,656-26,992,376 , GRCh37.p13 chr18: 24,571,620-24,572,340 CHST9
    nsv5882401copy number variation1nstd209human GRCh38 chr18: 26,995,941-27,000,791 , GRCh37.p13 chr18: 24,575,905-24,580,755 CHST9
    nsv5881426copy number variation1nstd209human GRCh38 chr18: 26,975,626-26,977,062 , GRCh37.p13 chr18: 24,555,590-24,557,026 CHST9
    nsv5876342copy number variation1nstd209human GRCh38 chr18: 27,062,481-27,070,296 , GRCh37.p13 chr18: 24,642,445-24,650,260 CHST9, LOC105372036
    nsv5869063copy number variation1nstd209human GRCh38 chr18: 27,097,387-27,101,186 , GRCh37.p13 chr18: 24,677,351-24,681,150 CHST9
    nsv5730525mobile element insertion1nstd211human GRCh38 chr18: 27,089,828-27,089,828 , GRCh37.p13 chr18: 24,669,792-24,669,792 CHST9
    nsv5725107mobile element insertion1nstd211human GRCh38 chr18: 26,956,727-26,956,727 , GRCh37.p13 chr18: 24,536,691-24,536,691 CHST9
    nsv5717977mobile element insertion1nstd211human GRCh38 chr18: 27,014,671-27,014,671 , GRCh37.p13 chr18: 24,594,635-24,594,635 CHST9
    nsv5713468mobile element insertion1nstd211human GRCh38 chr18: 27,010,811-27,010,811 , GRCh37.p13 chr18: 24,590,775-24,590,775 CHST9
    nsv5708283mobile element insertion1nstd211human GRCh38 chr18: 26,965,888-26,965,888 , GRCh37.p13 chr18: 24,545,852-24,545,852 CHST9
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