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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7059980inversion1nstd229human GRCh38 chr20: 30,656,049-33,860,963 , GRCh37.p13 chr20: 29,803,910-32,448,769 NECAB3, EFCAB8, 98 more genes
    nsv7037634copy number variation1nstd229human GRCh38 chr20: 32,691,987-32,709,492 , GRCh37.p13 chr20: 31,279,789-31,297,294 COMMD7
    nsv7037422copy number variation1nstd229human GRCh38 chr20: 32,732,690-32,735,678 , GRCh37.p13 chr20: 31,320,497-31,323,485 COMMD7
    nsv7035986copy number variation1nstd229human GRCh38 chr20: 32,708,600-32,712,631 , GRCh37.p13 chr20: 31,296,402-31,300,433 COMMD7
    nsv7030230copy number variation1nstd229human GRCh38 chr20: 32,700,954-32,701,210 , GRCh37.p13 chr20: 31,288,756-31,289,012 COMMD7
    nsv7030061copy number variation1nstd229human GRCh38 chr20: 32,654,026-32,741,076 , GRCh37.p13 chr20: 31,241,828-31,328,882 C20orf203, COMMD7, 1 more genes
    nsv7028368copy number variation1nstd229human GRCh38 chr20: 31,579,910-33,642,127 , GRCh37.p13 chr20: 30,167,713-32,229,933 PLAGL2, BPIFB4, 57 more genes
    nsv7018773copy number variation1nstd229human GRCh38 chr20: 32,518,401-32,743,500 , GRCh37.p13 chr20: 31,106,204-31,331,306 C20orf203, LOC101929698, 5 more genes
    nsv7018119copy number variation1nstd229human GRCh38 chr20: 32,744,400-32,746,441 , GRCh37.p13 chr20: 31,332,206-31,334,247 COMMD7
    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
    nsv6598853inversion1nstd223human GRCh38 chr20: 32,705,528-32,706,043 , GRCh37.p13 chr20: 31,293,330-31,293,845 COMMD7
    nsv6534220copy number variation1nstd223human GRCh38 chr20: 32,716,606-32,720,829 , GRCh37.p13 chr20: 31,304,408-31,308,632 COMMD7
    nsv6532451copy number variation1nstd223human GRCh38 chr20: 32,715,771-32,716,579 , GRCh37.p13 chr20: 31,303,573-31,304,381 COMMD7
    nsv6529985copy number variation1nstd223human GRCh38 chr20: 32,701,117-32,769,216 , GRCh37.p13 chr20: 31,288,919-31,357,022 COMMD7, DNMT3B
    nsv6529276copy number variation1nstd223human GRCh38 chr20: 32,734,994-32,735,788 , GRCh37.p13 chr20: 31,322,801-31,323,595 COMMD7
    nsv6529143copy number variation1nstd223human GRCh38 chr20: 32,712,103-32,720,328 , GRCh37.p13 chr20: 31,299,905-31,308,131 COMMD7
    nsv6528602copy number variation1nstd223human GRCh38 chr20: 32,734,390-32,742,387 , GRCh37.p13 chr20: 31,322,197-31,330,193 COMMD7
    nsv6524903copy number variation1nstd223human GRCh38 chr20: 32,700,954-32,701,210 , GRCh37.p13 chr20: 31,288,756-31,289,012 COMMD7
    nsv6523827copy number variation1nstd223human GRCh38 chr20: 32,739,555-32,740,227 , GRCh37.p13 chr20: 31,327,362-31,328,034 COMMD7
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