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Items: 1 to 20 of 342

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097029copy number variation1nstd102humanPathogenic GRCh37 chr5: 151,304,035-151,304,110 , GRCh38.p12 chr5: 151,924,474-151,924,549 GLRA1
    nsv7097028copy number variation1nstd102humanPathogenic GRCh37 chr5: 151,230,931-151,304,110 , GRCh38.p12 chr5: 151,851,370-151,924,549 TRQ-CTG13-1, GLULP1, 2 more genes
    nsv7097027copy number variation1nstd102humanUncertain significance GRCh37 chr5: 150,885,126-151,304,110 , GRCh38.p12 chr5: 151,505,565-151,924,549 CLMAT3, LOC100652758, 14 more genes
    nsv7096761copy number variation1nstd102humanUncertain significance GRCh37 chr5: 151,271,852-151,304,110 , GRCh38.p12 chr5: 151,892,291-151,924,549 GLRA1
    nsv7093370copy number variation1nstd102humannot provided GRCh37 chr5: 151,266,729-151,378,894 , GRCh38.p12 chr5: 151,887,168-151,999,333 LINC01933, GLRA1
    nsv7053998inversion1nstd229human GRCh38 chr5: 148,749,982-154,424,819 , GRCh37.p13 chr5: 148,129,545-153,804,379 HMGXB3, RN7SL868P, 102 more genes
    nsv7048662inversion1nstd229human GRCh38 chr5: 151,859,170-151,861,847 , GRCh37.p13 chr5: 151,238,731-151,241,408 GLRA1
    nsv7040531inversion1nstd229human GRCh38 chr5: 151,482,879-155,518,141 , GRCh37.p13 chr5: 150,862,440-154,897,701 RN7SL803P, MRPL22, 56 more genes
    nsv7040060inversion1nstd229human GRCh38 chr5: 151,920,229-151,970,438 , GRCh37.p13 chr5: 151,299,790-151,349,999 GLRA1, LINC01933
    nsv6797345copy number variation1nstd229human GRCh38 chr5: 151,854,114-151,857,226 , GRCh37.p13 chr5: 151,233,675-151,236,787 GLRA1
    nsv6794482copy number variation1nstd229human GRCh38 chr5: 151,815,611-151,827,586 , GRCh37.p13 chr5: 151,195,172-151,207,147 GLRA1
    nsv6794073copy number variation1nstd229human GRCh38 chr5: 151,891,641-151,990,893 , GRCh37.p13 chr5: 151,271,202-151,370,454 GLRA1, LINC01933
    nsv6790638copy number variation1nstd229human GRCh38 chr5: 151,877,970-151,887,949 , GRCh37.p13 chr5: 151,257,531-151,267,510 GLRA1
    nsv6790524copy number variation1nstd229human GRCh38 chr5: 151,909,747-151,923,044 , GRCh37.p13 chr5: 151,289,308-151,302,605 GLRA1
    nsv6786377copy number variation1nstd229human GRCh38 chr5: 151,925,301-151,929,900 , GRCh37.p13 chr5: 151,304,862-151,309,461 GLRA1
    nsv6785444copy number variation1nstd229human GRCh38 chr5: 151,920,713-151,920,926 , GRCh37.p13 chr5: 151,300,274-151,300,487 GLRA1
    nsv6785119copy number variation1nstd229human GRCh38 chr5: 151,869,519-151,873,452 , GRCh37.p13 chr5: 151,249,080-151,253,013 GLRA1
    nsv6779673copy number variation1nstd229human GRCh38 chr5: 151,886,290-151,889,969 , GRCh37.p13 chr5: 151,265,851-151,269,530 GLRA1
    nsv6778606copy number variation1nstd229human GRCh38 chr5: 151,860,401-151,867,100 , GRCh37.p13 chr5: 151,239,962-151,246,661 GLRA1, TRQ-CTG13-1
    nsv6636891copy number variation1nstd102humanPathogenic GRCh37 chr5: 150,535,183-172,906,793 , GRCh38.p12 chr5: 151,155,622-173,479,790 EFCAB9, LOC112267936, 287 more genes
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