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Items: 1 to 20 of 259

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7037579copy number variation1nstd229human GRCh38 chr20: 34,986,109-34,996,364 , GRCh37.p13 chr20: 33,573,912-33,584,167 MIR499B, MIR499A, 1 more genes
    nsv7036314copy number variation1nstd229human GRCh38 chr20: 34,999,064-35,002,110 , GRCh37.p13 chr20: 33,586,867-33,589,913 MYH7B, TRPC4AP
    nsv7033814copy number variation1nstd229human GRCh38 chr20: 34,955,464-34,963,037 , GRCh37.p13 chr20: 33,543,267-33,550,840 GSS, MYH7B
    nsv7030482copy number variation1nstd229human GRCh38 chr20: 35,002,127-35,002,314 , GRCh37.p13 chr20: 33,589,930-33,590,117 MYH7B, TRPC4AP
    nsv7029258copy number variation1nstd229human GRCh38 chr20: 34,997,382-34,998,292 , GRCh37.p13 chr20: 33,585,185-33,586,095 MYH7B
    nsv7025822copy number variation1nstd229human GRCh38 chr20: 34,970,177-34,970,608 , GRCh37.p13 chr20: 33,557,980-33,558,411 MYH7B
    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
    nsv7023730copy number variation1nstd229human GRCh38 chr20: 34,987,465-34,988,082 , GRCh37.p13 chr20: 33,575,268-33,575,885 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
    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
    nsv6524124copy number variation1nstd223human GRCh38 chr20: 34,958,585-34,959,559 , GRCh37.p13 chr20: 33,546,388-33,547,362 MYH7B
    nsv6522340copy number variation1nstd223human GRCh38 chr20: 34,987,466-34,987,996 , GRCh37.p13 chr20: 33,575,269-33,575,799 MYH7B
    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
    nsv6220749copy number variation1nstd214human GRCh38 chr20: 34,973,790-34,973,956 , GRCh37.p13 chr20: 33,561,593-33,561,759 MYH7B
    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
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