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Items: 1 to 20 of 144

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147429insertion1nstd232human GRCh37.p13 chr20: 34,145,020-34,145,020 , GRCh38.p12 chr20: 35,557,249-35,557,249 ERGIC3, FER1L4
    nsv7143854copy number variation1nstd232human GRCh37.p13 chr20: 34,143,898-34,143,974 , GRCh38.p12 chr20: 35,556,127-35,556,203 ERGIC3
    nsv7142904insertion1nstd232human GRCh37.p13 chr20: 34,130,690-34,130,690 , GRCh38.p12 chr20: 35,542,941-35,542,941 ERGIC3, RPL36P4
    nsv7141339copy number variation1nstd232human GRCh37.p13 chr20: 34,130,140-34,130,258 , GRCh38.p12 chr20: 35,542,391-35,542,509 ERGIC3, RPL36P4
    nsv7139804copy number variation1nstd232human GRCh37.p13 chr20: 34,144,877-34,144,960 , GRCh38.p12 chr20: 35,557,106-35,557,189 ERGIC3, FER1L4
    nsv7031265copy number variation1nstd229human GRCh38 chr20: 35,555,075-35,556,032 , GRCh37.p13 chr20: 34,142,846-34,143,803 ERGIC3
    nsv7024420copy number variation1nstd229human GRCh38 chr20: 35,548,903-35,595,731 , GRCh37.p13 chr20: 34,136,656-34,183,653 RPL37P1, ERGIC3, 1 more genes
    nsv7022193copy number variation1nstd229human GRCh38 chr20: 35,536,224-35,542,399 , GRCh37.p13 chr20: 34,124,048-34,130,148 RPL36P4, ERGIC3
    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
    nsv7019999copy number variation1nstd229human GRCh38 chr20: 35,486,342-36,114,422 , GRCh37.p13 chr20: 34,074,168-34,702,344 HMGB3P2, NFS1, 24 more genes
    nsv7018548copy number variation1nstd229human GRCh38 chr20: 35,548,069-35,551,651 , GRCh37.p13 chr20: 34,135,822-34,139,405 ERGIC3
    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
    nsv6597534inversion1nstd223human GRCh38 chr20: 35,544,970-35,545,452 , GRCh37.p13 chr20: 34,132,721-34,133,203 ERGIC3, RPL36P4
    nsv6311078copy number variation1nstd102humanPathogenic GRCh37 chr20: 31,189,994-34,287,210 , GRCh38.p12 chr20: 32,602,192-35,699,288 EDEM2, EIF2S2, 93 more genes
    nsv6133913copy number variation1nstd213human GRCh37 chr20: 33,870,000-34,270,001 , GRCh38.p12 chr20: 35,282,197-35,682,079 EIF6, GDF5, 18 more genes
    nsv5022343copy number variation1nstd200human GRCh38 chr20: 32,602,560-45,347,064 , GRCh37.p13 chr20: 31,190,362-43,975,704 , SNHG11, 286 more genes
    nsv5022342copy number variation1nstd200human GRCh38 chr20: 32,576,247-46,538,786 , GRCh37.p13 chr20: 31,164,049-45,167,425 , NECAB3, 350 more genes
    nsv5022326copy number variation1nstd200human GRCh38 chr20: 32,216,214-44,981,731 , GRCh37.p13 chr20: 30,804,017-43,610,372 , HNF4A, 279 more genes
    nsv4868593copy number variation1nstd200human GRCh37 chr20: 31,164,049-45,167,425 , GRCh38.p12 chr20: 32,576,247-46,538,786 , MMP24-AS1-EDEM2, 350 more genes
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