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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144459insertion1nstd232human GRCh37.p13 chr20: 33,621,665-33,621,665 , GRCh38.p12 chr20: 35,033,862-35,033,862 TRPC4AP
    nsv7143794insertion1nstd232human GRCh37.p13 chr20: 33,632,517-33,632,517 , GRCh38.p12 chr20: 35,044,714-35,044,714 TRPC4AP
    nsv7141795insertion1nstd232human GRCh37.p13 chr20: 33,628,861-33,628,861 , GRCh38.p12 chr20: 35,041,058-35,041,058 TRPC4AP
    nsv7036314copy number variation1nstd229human GRCh38 chr20: 34,999,064-35,002,110 , GRCh37.p13 chr20: 33,586,867-33,589,913 MYH7B, TRPC4AP
    nsv7036268copy number variation1nstd229human GRCh38 chr20: 35,092,817-35,099,313 , GRCh37.p13 chr20: 33,680,620-33,687,116 TRPC4AP
    nsv7035841copy number variation1nstd229human GRCh38 chr20: 35,030,901-35,033,300 , GRCh37.p13 chr20: 33,618,704-33,621,103 TRPC4AP, RNU6-407P
    nsv7033015copy number variation1nstd229human GRCh38 chr20: 35,041,058-35,041,154 , GRCh37.p13 chr20: 33,628,861-33,628,957 TRPC4AP
    nsv7032005copy number variation1nstd229human GRCh38 chr20: 35,062,244-35,070,322 , GRCh37.p13 chr20: 33,650,047-33,658,125 TRPC4AP
    nsv7031769copy number variation1nstd229human GRCh38 chr20: 35,048,620-35,048,794 , GRCh37.p13 chr20: 33,636,423-33,636,597 TRPC4AP
    nsv7030482copy number variation1nstd229human GRCh38 chr20: 35,002,127-35,002,314 , GRCh37.p13 chr20: 33,589,930-33,590,117 MYH7B, TRPC4AP
    nsv7028568copy number variation1nstd229human GRCh38 chr20: 35,058,640-35,066,007 , GRCh37.p13 chr20: 33,646,443-33,653,810 TRPC4AP
    nsv7024755copy number variation1nstd229human GRCh38 chr20: 34,981,260-35,029,451 , GRCh37.p13 chr20: 33,569,063-33,617,254 MYH7B, MIR499B, 3 more genes
    nsv7023578copy number variation1nstd229human GRCh38 chr20: 35,033,835-35,034,157 , GRCh37.p13 chr20: 33,621,638-33,621,960 TRPC4AP
    nsv7022737copy number variation1nstd229human GRCh38 chr20: 34,899,761-35,090,256 , GRCh37.p13 chr20: 33,487,564-33,678,059 ACSS2, RNU6-407P, 5 more genes
    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
    nsv7018321copy number variation1nstd229human GRCh38 chr20: 35,080,242-35,108,478 , GRCh37.p13 chr20: 33,668,045-33,696,281 TRPC4AP
    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
    nsv6599659inversion1nstd223human GRCh38 chr20: 35,066,451-35,067,218 , GRCh37.p13 chr20: 33,654,254-33,655,021 TRPC4AP
    nsv6599613inversion1nstd223human GRCh38 chr20: 35,086,125-35,086,545 , GRCh37.p13 chr20: 33,673,928-33,674,348 TRPC4AP
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