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Items: 1 to 20 of 231

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076785inversion1nstd229human GRCh38 chr20: 36,001,722-37,069,571 , GRCh37.p13 chr20: 34,589,644-35,697,974 RPS3AP3, EPB41L1-AS1, 22 more genes
    nsv7037168copy number variation1nstd229human GRCh38 chr20: 36,626,948-36,627,012 , GRCh37.p13 chr20: 35,255,351-35,255,415 SLA2
    nsv7032589copy number variation1nstd229human GRCh38 chr20: 36,635,566-36,639,432 , GRCh37.p13 chr20: 35,263,969-35,267,835 SLA2
    nsv7026973copy number variation1nstd229human GRCh38 chr20: 36,612,001-36,614,400 , GRCh37.p13 chr20: 35,240,404-35,242,803 SLA2, TGIF2-RAB5IF, 1 more genes
    nsv7025008copy number variation1nstd229human GRCh38 chr20: 36,623,278-36,625,976 , GRCh37.p13 chr20: 35,251,681-35,254,379 SLA2
    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
    nsv7019194copy number variation1nstd229human GRCh38 chr20: 36,620,325-36,621,064 , GRCh37.p13 chr20: 35,248,728-35,249,467 SLA2, HNRNPA3P2
    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
    nsv6599958inversion1nstd223human GRCh38 chr20: 36,620,432-36,620,581 , GRCh37.p13 chr20: 35,248,835-35,248,984 SLA2, HNRNPA3P2
    nsv6598784inversion1nstd223human GRCh38 chr20: 36,616,461-36,616,929 , GRCh37.p13 chr20: 35,244,864-35,245,332 SLA2
    nsv6528052copy number variation1nstd223human GRCh38 chr20: 36,607,463-36,620,882 , GRCh37.p13 chr20: 35,235,866-35,249,285 SLA2, HNRNPA3P2, 2 more genes
    nsv6134023copy number variation1nstd213human GRCh37 chr20: 34,270,000-35,840,001 , GRCh38.p12 chr20: 35,682,078-37,211,598 RBL1, AAR2, 35 more genes
    nsv6128117copy number variation1nstd186human GRCh37 chr20: 35,264,591-35,264,845 , GRCh38.p12 chr20: 36,636,188-36,636,442 SLA2
    nsv6105590insertion1nstd212human GRCh38 chr20: 36,642,167-36,642,167 , GRCh37.p13 chr20: 35,270,570-35,270,570 SLA2
    nsv6057785copy number variation1nstd212human GRCh38 chr20: 36,637,270-36,637,357 , GRCh37.p13 chr20: 35,265,673-35,265,760 SLA2
    nsv6052586copy number variation1nstd212human GRCh38 chr20: 36,641,900-36,642,183 , GRCh37.p13 chr20: 35,270,303-35,270,586 SLA2
    nsv6041505copy number variation1nstd212human GRCh38 chr20: 36,620,788-36,620,856 , GRCh37.p13 chr20: 35,249,191-35,249,259 SLA2, HNRNPA3P2
    nsv5975262insertion1nstd209human GRCh38 chr20: 36,642,163-36,642,163 , GRCh37.p13 chr20: 35,270,566-35,270,566 SLA2
    nsv5965797copy number variation1nstd209human GRCh38 chr20: 36,637,171-36,637,221 , GRCh37.p13 chr20: 35,265,574-35,265,624 SLA2
    nsv5953998copy number variation1nstd209human GRCh38 chr20: 36,636,146-36,636,675 , GRCh37.p13 chr20: 35,264,549-35,265,078 SLA2
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