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Items: 1 to 20 of 328

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7073871inversion1nstd229human GRCh38 chr20: 35,194,451-35,195,983 , GRCh37.p13 chr20: 33,782,254-33,783,786 MMP24-AS1-EDEM2, PROCR, 1 more genes
    nsv7070375inversion1nstd229human GRCh38 chr20: 35,199,059-35,203,692 , GRCh37.p13 chr20: 33,786,862-33,791,495 PROCR, MMP24-AS1-EDEM2
    nsv7068934inversion1nstd229human GRCh38 chr20: 35,190,934-35,194,452 , GRCh37.p13 chr20: 33,778,737-33,782,255 PROCR, RNA5SP483, 1 more genes
    nsv7036788copy number variation1nstd229human GRCh38 chr20: 35,139,687-35,171,665 , GRCh37.p13 chr20: 33,727,490-33,759,468 EDEM2, MMP24-AS1-EDEM2, 1 more genes
    nsv7036165copy number variation1nstd229human GRCh38 chr20: 35,165,999-35,171,826 , GRCh37.p13 chr20: 33,753,802-33,759,629 PROCR, MMP24-AS1-EDEM2
    nsv7035456copy number variation1nstd229human GRCh38 chr20: 35,170,258-35,170,461 , GRCh37.p13 chr20: 33,758,061-33,758,264 MMP24-AS1-EDEM2, PROCR
    nsv7032159copy number variation1nstd229human GRCh38 chr20: 35,114,221-35,220,642 , GRCh37.p13 chr20: 33,702,024-33,808,445 MT1P3, RNA5SP483, 3 more genes
    nsv7029836copy number variation1nstd229human GRCh38 chr20: 35,204,901-35,211,600 , GRCh37.p13 chr20: 33,792,704-33,799,403 MMP24-AS1-EDEM2, PROCR
    nsv7029384copy number variation1nstd229human GRCh38 chr20: 35,182,000-35,188,039 , GRCh37.p13 chr20: 33,769,803-33,775,842 PROCR, MMP24-AS1-EDEM2
    nsv7025007copy number variation1nstd229human GRCh38 chr20: 35,211,877-35,222,102 , GRCh37.p13 chr20: 33,799,680-33,809,905 MMP24-AS1-EDEM2, MT1P3, 1 more genes
    nsv7023400copy number variation1nstd229human GRCh38 chr20: 35,174,828-35,182,089 , GRCh37.p13 chr20: 33,762,631-33,769,892 PROCR, MMP24-AS1-EDEM2
    nsv7022130copy number variation1nstd229human GRCh38 chr20: 35,175,401-35,207,400 , GRCh37.p13 chr20: 33,763,204-33,795,203 PROCR, RNA5SP483, 1 more genes
    nsv7021198copy number variation1nstd229human GRCh38 chr20: 33,145,032-41,995,765 , GRCh37.p13 chr20: 31,732,838-40,624,405 PXMP4, RPL12P11, 199 more genes
    nsv7020037copy number variation1nstd229human GRCh38 chr20: 35,166,772-35,176,647 , GRCh37.p13 chr20: 33,754,575-33,764,450 MMP24-AS1-EDEM2, PROCR
    nsv7019952copy number variation1nstd229human GRCh38 chr20: 35,195,485-35,200,487 , GRCh37.p13 chr20: 33,783,288-33,788,290 PROCR, RNA5SP483, 1 more genes
    nsv7018533copy number variation1nstd229human GRCh38 chr20: 35,188,187-35,213,315 , GRCh37.p13 chr20: 33,775,990-33,801,118 RNA5SP483, PROCR, 1 more genes
    nsv6637725copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 29,833,535-34,815,537 , GRCh38.p12 chr20: 31,245,732-36,227,615 AHCY, ASIP, 160 more genes
    nsv6637546copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 29,652,122-35,603,726 , GRCh38.p12 chr20: 30,417,446-36,975,323 AHCY, ASIP, 195 more genes
    nsv6598923inversion1nstd223human GRCh38 chr20: 35,214,405-35,214,919 , GRCh37.p13 chr20: 33,802,208-33,802,722 MMP24-AS1-EDEM2, PROCR
    nsv6597558inversion1nstd223human GRCh38 chr20: 35,214,023-35,214,978 , GRCh37.p13 chr20: 33,801,826-33,802,781 PROCR, MMP24-AS1-EDEM2
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