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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
    nsv7037047copy number variation1nstd229human GRCh38 chr20: 22,675,169-22,677,769 , GRCh37.p13 chr20: 22,655,807-22,658,407 LINC01747
    nsv7028027copy number variation1nstd229human GRCh38 chr20: 22,681,478-22,681,858 , GRCh37.p13 chr20: 22,662,116-22,662,496 LINC01747
    nsv7025748copy number variation1nstd229human GRCh38 chr20: 22,674,201-22,679,400 , GRCh37.p13 chr20: 22,654,839-22,660,038 LINC01747
    nsv7019573copy number variation1nstd229human GRCh38 chr20: 22,680,239-22,694,542 , GRCh37.p13 chr20: 22,660,877-22,675,180 LINC01747
    nsv6599430inversion1nstd223human GRCh38 chr20: 22,674,842-22,675,815 , GRCh37.p13 chr20: 22,655,480-22,656,453 LINC01747
    nsv6596962inversion1nstd223human GRCh38 chr20: 22,685,082-22,692,451 , GRCh37.p13 chr20: 22,665,720-22,673,089 LINC01747
    nsv6530961copy number variation1nstd223human GRCh38 chr20: 22,685,082-22,689,442 , GRCh37.p13 chr20: 22,665,720-22,670,080 LINC01747
    nsv6526926copy number variation1nstd223human GRCh38 chr20: 22,674,684-22,675,012 , GRCh37.p13 chr20: 22,655,322-22,655,650 LINC01747
    nsv6523073copy number variation1nstd223human GRCh38 chr20: 22,671,968-22,693,138 , GRCh37.p13 chr20: 22,652,606-22,673,776 LINC01747
    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
    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
    nsv6123329copy number variation1nstd186human GRCh37 chr20: 22,655,339-22,655,650 , GRCh38.p12 chr20: 22,674,701-22,675,012 LINC01747
    nsv6059162copy number variation1nstd212human GRCh38 chr20: 22,674,684-22,675,012 , GRCh37.p13 chr20: 22,655,322-22,655,650 LINC01747
    nsv5955038copy number variation1nstd209human GRCh38 chr20: 22,674,684-22,675,011 , GRCh37.p13 chr20: 22,655,322-22,655,649 LINC01747
    nsv5947618copy number variation1nstd209human GRCh38 chr20: 22,665,530-22,683,354 , GRCh37.p13 chr20: 22,646,168-22,663,992 LINC01747
    nsv5883545copy number variation2nstd209human GRCh38 chr20: 22,677,451-22,678,550 , GRCh37.p13 chr20: 22,658,089-22,659,188 LINC01747
    nsv5882486copy number variation1nstd209human GRCh38 chr20: 22,676,051-22,677,150 , GRCh37.p13 chr20: 22,656,689-22,657,788 LINC01747
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