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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7049357inversion1nstd229human GRCh38 chr3: 71,727,285-71,727,404 , GRCh37.p13 chr3: 71,776,436-71,776,555 EIF4E3
    nsv6716442copy number variation1nstd229human GRCh38 chr3: 71,748,101-71,828,900 , GRCh37.p13 chr3: 71,797,252-71,878,051 GPR27, EIF4E3, 3 more genes
    nsv6713745copy number variation1nstd229human GRCh38 chr3: 71,711,939-71,715,611 , GRCh37.p13 chr3: 71,761,090-71,764,762 EIF4E3
    nsv6712385copy number variation1nstd229human GRCh38 chr3: 66,065,527-73,237,527 , GRCh37.p13 chr3: 66,051,202-73,286,678 , RNA5SP136, 79 more genes
    nsv6711975copy number variation1nstd229human GRCh38 chr3: 71,749,201-71,836,000 , GRCh37.p13 chr3: 71,798,352-71,885,151 LOC105377156, PROK2, 3 more genes
    nsv6706898copy number variation1nstd229human GRCh38 chr3: 71,324,286-71,720,341 , GRCh37.p13 chr3: 71,373,437-71,769,492 FOXP1, LOC105377155, 2 more genes
    nsv6706018copy number variation1nstd229human GRCh38 chr3: 71,130,830-71,734,980 , GRCh37.p13 chr3: 71,179,981-71,784,131 FOXP1-AS1, EIF4E3, 3 more genes
    nsv6699444copy number variation1nstd229human GRCh38 chr3: 71,570,336-71,712,859 , GRCh37.p13 chr3: 71,619,487-71,762,010 EIF4E3, FOXP1, 1 more genes
    nsv6699214copy number variation1nstd229human GRCh38 chr3: 71,748,674-71,748,760 , GRCh37.p13 chr3: 71,797,825-71,797,911 EIF4E3
    nsv6375131copy number variation1nstd223human GRCh38 chr3: 71,750,301-71,755,400 , GRCh37.p13 chr3: 71,799,452-71,804,551 EIF4E3, GPR27
    nsv6373171copy number variation1nstd223human GRCh38 chr3: 71,752,401-71,755,000 , GRCh37.p13 chr3: 71,801,552-71,804,151 GPR27, EIF4E3
    nsv6365532copy number variation1nstd223human GRCh38 chr3: 71,130,830-71,734,979 , GRCh37.p13 chr3: 71,179,981-71,784,130 FOXP1, MIR1284, 3 more genes
    nsv6134705copy number variation1nstd213human GRCh37 chr3: 66,270,000-87,730,001 , GRCh38.p12 chr3: 66,219,846-87,680,851 , AKR1B1P2, 187 more genes
    nsv5902904copy number variation1nstd209human GRCh38 chr3: 66,803,410-74,489,186 , GRCh37.p13 chr3: 66,853,834-74,538,337 , LOC105377160, 83 more genes
    nsv5836785copy number variation1nstd209human GRCh38 chr3: 71,725,648-71,726,995 , GRCh37.p13 chr3: 71,774,799-71,776,146 EIF4E3
    nsv5836479copy number variation1nstd209human GRCh38 chr3: 71,683,556-71,684,555 , GRCh37.p13 chr3: 71,732,707-71,733,706 EIF4E3
    nsv5836478copy number variation1nstd209human GRCh38 chr3: 71,677,056-71,678,155 , GRCh37.p13 chr3: 71,726,207-71,727,306 EIF4E3
    nsv5687377mobile element insertion2nstd211human GRCh38 chr3: 71,732,393-71,732,393 , GRCh37.p13 chr3: 71,781,544-71,781,544 EIF4E3
    nsv5564432copy number variation1nstd102humanPathogenic GRCh37 chr3: 68,939,251-72,700,418 , GRCh38.p12 chr3: 68,890,100-72,651,267 CCDC137P1, LOC105377160, 39 more genes
    nsv5534192insertion1nstd206human GRCh38 chr3: 71,685,724-71,685,756 , GRCh37.p13 chr3: 71,734,875-71,734,907 EIF4E3
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