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Items: 1 to 20 of 251

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5972031insertion1nstd209human GRCh38 chr12: 53,030,413-53,030,413 , GRCh37.p13 chr12: 53,424,197-53,424,197 EIF4B
    nsv5970103insertion1nstd209human GRCh38 chr12: 53,027,136-53,027,136 , GRCh37.p13 chr12: 53,420,920-53,420,920 EIF4B
    nsv5931893copy number variation1nstd209human GRCh38 chr12: 53,030,066-53,030,225 , GRCh37.p13 chr12: 53,423,850-53,424,009 EIF4B
    nsv5657074insertion1nstd207human GRCh38 chr12: 53,042,184-53,042,184 , GRCh37.p13 chr12: 53,435,968-53,435,968 TNS2-AS1, EIF4B
    nsv5587850copy number variation1nstd207human GRCh38 chr12: 53,030,063-53,030,222 , GRCh37.p13 chr12: 53,423,847-53,424,006 EIF4B
    nsv5391009copy number variation1nstd186human GRCh37 chr12: 53,423,887-53,424,071 , GRCh38.p12 chr12: 53,030,103-53,030,287 EIF4B
    nsv5272509copy number variation1nstd204human GRCh38.p13 chr12: 53,002,810-53,008,289 , GRCh37.p13 chr12: 53,396,594-53,402,073 EIF4B
    nsv5138559mobile element insertion1nstd203human GRCh38 chr12: 53,035,986-53,035,986 , GRCh37.p13 chr12: 53,429,770-53,429,770 EIF4B
    nsv5138310mobile element insertion1nstd203human GRCh38 chr12: 53,035,961-53,035,987 , GRCh37.p13 chr12: 53,429,745-53,429,771 EIF4B
    nsv5135898mobile element insertion1nstd203human GRCh38 chr12: 53,019,441-53,019,474 , GRCh37.p13 chr12: 53,413,225-53,413,258 EIF4B
    nsv5134590mobile element insertion1nstd203human GRCh38 chr12: 53,030,418-53,030,436 , GRCh37.p13 chr12: 53,424,202-53,424,220 EIF4B
    nsv5131414mobile element insertion1nstd203human GRCh38 chr12: 53,035,982-53,035,992 , GRCh37.p13 chr12: 53,429,766-53,429,776 EIF4B
    nsv5130548mobile element insertion1nstd203human GRCh38 chr12: 53,035,987-53,035,991 , GRCh37.p13 chr12: 53,429,771-53,429,775 EIF4B
    nsv5128551mobile element insertion1nstd203human GRCh38 chr12: 53,030,417-53,030,438 , GRCh37.p13 chr12: 53,424,201-53,424,222 EIF4B
    nsv5127805mobile element insertion1nstd203human GRCh38 chr12: 53,035,985-53,035,992 , GRCh37.p13 chr12: 53,429,769-53,429,776 EIF4B
    nsv5125884mobile element insertion1nstd203human GRCh38 chr12: 53,035,945-53,035,987 , GRCh37.p13 chr12: 53,429,729-53,429,771 EIF4B
    nsv5124140mobile element insertion1nstd203human GRCh38 chr12: 53,030,413-53,030,425 , GRCh37.p13 chr12: 53,424,197-53,424,209 EIF4B
    nsv5123599mobile element insertion1nstd203human GRCh38 chr12: 53,035,991-53,035,991 , GRCh37.p13 chr12: 53,429,775-53,429,775 EIF4B
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
    nsv5036282inversion1nstd200human GRCh38 chr12: 52,338,357-95,425,642 , GRCh37.p13 chr12: 52,732,141-95,819,418 , MIR6502, 769 more genes
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