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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076766inversion1nstd229human GRCh38 chr20: 31,354,223-31,381,977 , GRCh37.p13 chr20: 29,942,026-29,969,780 DEFB119, DEFB118, 2 more genes
    nsv7059980inversion1nstd229human GRCh38 chr20: 30,656,049-33,860,963 , GRCh37.p13 chr20: 29,803,910-32,448,769 NECAB3, EFCAB8, 98 more genes
    nsv7034414copy number variation1nstd229human GRCh38 chr20: 31,261,380-31,438,822 , GRCh37.p13 chr20: 29,849,183-30,026,625 DEFB121, DEFB117, 10 more genes
    nsv7033985copy number variation1nstd229human GRCh38 chr20: 31,342,847-31,399,632 , GRCh37.p13 chr20: 29,930,650-29,987,435 DEFB118, DEFB119, 3 more genes
    nsv7032945copy number variation1nstd229human GRCh38 chr20: 31,283,144-31,615,397 , GRCh37.p13 chr20: 29,870,947-30,203,200 HM13-AS1, DEFB119, 22 more genes
    nsv7032549copy number variation1nstd229human GRCh38 chr20: 31,308,013-31,715,090 , GRCh37.p13 chr20: 29,895,816-30,302,893 TRS-AGA7-1, ID1, 24 more genes
    nsv7021866copy number variation1nstd229human GRCh38 chr20: 31,358,039-31,410,913 , GRCh37.p13 chr20: 29,945,842-29,998,716 DEFB119, DEFB118, 2 more genes
    nsv7019601copy number variation1nstd229human GRCh38 chr20: 31,354,652-31,414,258 , GRCh37.p13 chr20: 29,942,455-30,002,061 DEFB119, DEFB118, 3 more genes
    nsv7019583copy number variation1nstd229human GRCh38 chr20: 31,380,201-31,401,300 , GRCh37.p13 chr20: 29,968,004-29,989,103 DEFB119
    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
    nsv6626562copy number variation1nstd224human GRCh37 chr20: 29,811,475-30,242,490 , GRCh38.p12 chr20: 31,223,672-31,654,687 CD24P3, DKKL1P1, 25 more genes
    nsv6626339copy number variation2nstd224human GRCh37 chr20: 29,833,609-30,070,197 , GRCh38.p12 chr20: 31,245,806-31,482,394 REM1, DEFB118, 13 more genes
    nsv6529120copy number variation1nstd223human GRCh38 chr20: 31,377,595-31,378,218 , GRCh37.p13 chr20: 29,965,398-29,966,021 DEFB119
    nsv6519900copy number variation1nstd223human GRCh38 chr20: 31,380,231-31,401,279 , GRCh37.p13 chr20: 29,968,034-29,989,082 DEFB119
    nsv6517967copy number variation1nstd223human GRCh38 chr20: 31,354,652-31,414,258 , GRCh37.p13 chr20: 29,942,455-30,002,061 DEFB118, RNA5SP480, 3 more genes
    nsv6313956copy number variation1nstd102humanPathogenic GRCh37 chr20: 25,442,597-33,761,550 , GRCh38.p12 chr20: 25,461,961-35,173,747 LOC105372586, RNU6-384P, 193 more genes
    nsv6291672copy number variation1nstd102humanLikely benign GRCh37 chr20: 29,652,122-30,272,637 , GRCh38.p12 chr20: 30,417,446-31,684,834 DEFB124, LOC105379481, 47 more genes
    nsv6291590copy number variation1nstd102humanLikely benign GRCh37 chr20: 29,652,122-30,518,304 , GRCh38.p12 chr20: 30,417,446-31,930,501 CDC27P4, DEFB122, 54 more genes
    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
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