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Items: 1 to 20 of 198

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7037990copy number variation1nstd229human GRCh38 chr20: 34,942,630-34,942,795 , GRCh37.p13 chr20: 33,530,433-33,530,598 GSS
    nsv7033814copy number variation1nstd229human GRCh38 chr20: 34,955,464-34,963,037 , GRCh37.p13 chr20: 33,543,267-33,550,840 GSS, MYH7B
    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
    nsv7018637copy number variation1nstd229human GRCh38 chr20: 34,922,687-34,931,170 , GRCh37.p13 chr20: 33,510,490-33,518,973 ACSS2, GSS
    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
    nsv6626565copy number variation1nstd224human GRCh37 chr20: 33,488,771-33,551,100 , GRCh38.p12 chr20: 34,900,968-34,963,297 MYH7B, ACSS2, 1 more genes
    nsv6599561inversion1nstd223human GRCh38 chr20: 34,933,994-34,934,415 , GRCh37.p13 chr20: 33,521,797-33,522,218 GSS
    nsv6597097inversion1nstd223human GRCh38 chr20: 34,938,973-34,939,751 , GRCh37.p13 chr20: 33,526,776-33,527,554 GSS
    nsv6525888copy number variation1nstd223human GRCh38 chr20: 34,952,641-34,953,743 , GRCh37.p13 chr20: 33,540,444-33,541,546 GSS
    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
    nsv6109428insertion1nstd212human GRCh38 chr20: 34,950,035-34,950,035 , GRCh37.p13 chr20: 33,537,838-33,537,838 GSS
    nsv6109414insertion1nstd212human GRCh38 chr20: 34,934,177-34,934,177 , GRCh37.p13 chr20: 33,521,980-33,521,980 GSS
    nsv6102976insertion1nstd212human GRCh38 chr20: 34,937,510-34,937,510 , GRCh37.p13 chr20: 33,525,313-33,525,313 GSS
    nsv6053195copy number variation1nstd212human GRCh38 chr20: 34,934,418-34,934,514 , GRCh37.p13 chr20: 33,522,221-33,522,317 GSS
    nsv5978979insertion1nstd209human GRCh38 chr20: 34,950,020-34,950,020 , GRCh37.p13 chr20: 33,537,823-33,537,823 GSS
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