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Items: 1 to 20 of 163

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7060544inversion1nstd229human GRCh38 chr20: 34,359,005-34,717,370 , GRCh37.p13 chr20: 32,946,811-33,305,174 FDX1P1, PIGU, 8 more genes
    nsv7035362copy number variation1nstd229human GRCh38 chr20: 34,549,301-34,556,100 , GRCh37.p13 chr20: 33,137,105-33,143,904 MAP1LC3A
    nsv7032912copy number variation1nstd229human GRCh38 chr20: 34,512,701-34,575,900 , GRCh37.p13 chr20: 33,100,506-33,163,704 PIGU, MAP1LC3A, 1 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
    nsv7020817copy number variation1nstd229human GRCh38 chr20: 34,558,760-34,558,790 , GRCh37.p13 chr20: 33,146,564-33,146,594 MAP1LC3A, PIGU
    nsv7019231copy number variation1nstd229human GRCh38 chr20: 34,550,854-34,552,988 , GRCh37.p13 chr20: 33,138,658-33,140,792 MAP1LC3A
    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
    nsv6596611inversion1nstd223human GRCh38 chr20: 34,551,294-34,551,585 , GRCh37.p13 chr20: 33,139,098-33,139,389 MAP1LC3A
    nsv6596304inversion1nstd223human GRCh38 chr20: 34,545,252-34,546,141 , GRCh37.p13 chr20: 33,133,056-33,133,945 MAP1LC3A
    nsv6518308copy number variation1nstd223human GRCh38 chr20: 34,538,206-34,545,408 , GRCh37.p13 chr20: 33,126,010-33,133,212 MAP1LC3A, DYNLRB1
    nsv6517724copy number variation1nstd223human GRCh38 chr20: 34,554,589-34,556,032 , GRCh37.p13 chr20: 33,142,393-33,143,836 MAP1LC3A
    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
    nsv6311078copy number variation1nstd102humanPathogenic GRCh37 chr20: 31,189,994-34,287,210 , GRCh38.p12 chr20: 32,602,192-35,699,288 EDEM2, EIF2S2, 93 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
    nsv6134288copy number variation1nstd213human GRCh37 chr20: 32,810,000-33,870,001 , GRCh38.p12 chr20: 34,222,194-35,282,198 AHCY, PROCR, 28 more genes
    nsv5952950copy number variation1nstd209human GRCh38 chr20: 34,143,842-34,843,201 , GRCh37.p13 chr20: 32,731,648-33,431,004 , AHCY, 15 more genes
    nsv5514096copy number variation1nstd206human GRCh38 chr20: 34,554,571-34,556,089 , GRCh37.p13 chr20: 33,142,375-33,143,893 MAP1LC3A
    nsv5329317translocation1nstd204human GRCh38.p13 chr20: 34,556,098-34,556,098 , GRCh38.p13 chr20: 34,555,795-34,555,795 , GRCh37.p13 chr20: 33,143,902-33,143,902 , GRCh37.p13 chr20: 33,143,599-33,143,599 MAP1LC3A
    nsv5163545mobile element insertion1nstd203human GRCh38 chr20: 34,554,352-34,554,393 , GRCh37.p13 chr20: 33,142,156-33,142,197 MAP1LC3A
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