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Items: 1 to 20 of 131

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148267copy number variation1nstd102humanPathogenic GRCh38 chr20: 87,153-23,635,465 , GRCh37.p13 chr20: 67,794-23,616,102 KRT18P3, RSPO4, 413 more genes
    nsv7071374inversion1nstd229human GRCh38 chr20: 22,578,336-22,578,536 , GRCh37.p13 chr20: 22,558,974-22,559,174 LINC00261
    nsv7029269copy number variation1nstd229human GRCh38 chr20: 22,561,487-22,568,578 , GRCh37.p13 chr20: 22,542,125-22,549,216 LINC00261
    nsv7027488copy number variation1nstd229human GRCh38 chr20: 22,549,040-22,560,820 , GRCh37.p13 chr20: 22,529,678-22,541,458 LINC00261
    nsv7026071copy number variation1nstd229human GRCh38 chr20: 22,574,529-22,574,705 , GRCh37.p13 chr20: 22,555,167-22,555,343 LINC00261
    nsv7024947copy number variation1nstd229human GRCh38 chr20: 22,561,015-22,564,867 , GRCh37.p13 chr20: 22,541,653-22,545,505 LINC00261
    nsv6291578copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 18,665,879-33,903,216 , GRCh38.p12 chr20: 18,685,235-35,315,413 AHCY, ASIP, 330 more genes
    nsv6288960insertion1nstd214human GRCh38 chr20: 22,561,933-22,561,933 , GRCh37.p13 chr20: 22,542,571-22,542,571 LINC00261
    nsv6288292insertion1nstd214human GRCh38 chr20: 22,561,937-22,561,937 , GRCh37.p13 chr20: 22,542,575-22,542,575 LINC00261
    nsv6286817insertion1nstd214human GRCh38 chr20: 22,561,914-22,561,914 , GRCh37.p13 chr20: 22,542,552-22,542,552 LINC00261
    nsv6134280copy number variation1nstd213human GRCh37 chr20: 22,530,000-23,650,001 , GRCh38.p12 chr20: 22,549,362-23,669,364 CST3, CYB5AP4, 33 more genes
    nsv6134279copy number variation1nstd213human GRCh37 chr20: 22,140,000-23,520,001 , GRCh38.p12 chr20: 22,159,362-23,539,364 RNA5SP478, LNCNEF, 34 more genes
    nsv6134275copy number variation1nstd213human GRCh37 chr20: 19,430,000-23,860,001 , GRCh38.p12 chr20: 19,449,356-23,879,364 CST1, CST4, 87 more genes
    nsv6134016copy number variation1nstd213human GRCh37 chr20: 22,350,000-22,600,001 , GRCh38.p12 chr20: 22,369,362-22,619,363 FOXA2, LINC00261, 5 more genes
    nsv6133799copy number variation1nstd213human GRCh37 chr20: 22,350,000-22,640,001 , GRCh38.p12 chr20: 22,369,362-22,659,363 FOXA2, LINC00261, 5 more genes
    nsv6106285insertion1nstd212human GRCh38 chr20: 22,561,929-22,561,929 , GRCh37.p13 chr20: 22,542,567-22,542,567 LINC00261
    nsv5973247insertion1nstd209human GRCh38 chr20: 22,561,929-22,561,929 , GRCh37.p13 chr20: 22,542,567-22,542,567 LINC00261
    nsv5870306copy number variation1nstd209human GRCh38 chr20: 22,578,489-22,597,803 , GRCh37.p13 chr20: 22,559,127-22,578,441 LINC00261, LNCNEF, 1 more genes
    nsv5667509insertion1nstd207human GRCh38 chr20: 22,561,914-22,561,914 , GRCh37.p13 chr20: 22,542,552-22,542,552 LINC00261
    nsv5322244copy number variation1nstd204human GRCh38.p13 chr20: 22,575,055-22,582,749 , GRCh37.p13 chr20: 22,555,693-22,563,387 LINC00261, FOXA2
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