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Items: 1 to 20 of 117

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5519147copy number variation1nstd206human GRCh38 chr20: 31,820,473-31,822,431 , GRCh37.p13 chr20: 30,408,276-30,410,234 MYLK2
    nsv5299835copy number variation1nstd204human GRCh38.p13 chr20: 31,818,044-31,851,651 , GRCh37.p13 chr20: 30,405,847-30,439,454 MYLK2, FOXS1, 1 more genes
    nsv5283549copy number variation1nstd204human GRCh38.p13 chr20: 31,227,801-32,548,400 , GRCh37.p13 chr20: 29,815,604-31,136,202 , XKR7, 52 more genes
    nsv5022316copy number variation1nstd200human GRCh38 chr20: 31,830,714-31,830,797 , GRCh37.p13 chr20: 30,418,517-30,418,600 MYLK2
    nsv4729837copy number variation1nstd102humanLikely benign GRCh37 chr20: 29,833,534-30,494,851 , GRCh38.p12 chr20: 31,245,731-31,907,048 DEFB117, LOC105372588, 34 more genes
    nsv4729757copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 19,750,804-30,479,077 , GRCh38.p12 chr20: 19,770,160-31,891,274 BCL2L1, CD24P3, 222 more genes
    nsv4668860copy number variation1nstd186human GRCh37 chr20: 30,408,349-30,411,103 , GRCh38.p12 chr20: 31,820,546-31,823,300 MYLK2
    nsv4632642copy number variation1nstd183human GRCh37 chr20: 29,835,049-30,626,430 , GRCh38.p12 chr20: 31,247,246-32,038,627 DEFB122, HAUS6P2, 38 more genes
    nsv4626606copy number variation1nstd183human GRCh37 chr20: 30,408,349-30,411,103 , GRCh38.p12 chr20: 31,820,546-31,823,300 MYLK2
    nsv4457806copy number variation1nstd102humanPathogenic GRCh37 chr20: 29,833,608-35,087,952 , GRCh38.p12 chr20: 31,245,805-36,459,549 EFCAB8, C20orf203, 162 more genes
    nsv4421039copy number variation1nstd174human GRCh37 chr20: 30,408,071-30,411,392 , GRCh38.p12 chr20: 31,820,268-31,823,589 MYLK2
    nsv4414329copy number variation1nstd174human GRCh37 chr20: 29,835,037-30,621,271 , GRCh38.p12 chr20: 31,247,234-32,033,468 CD24P3, DEFB118, 38 more genes
    nsv4280492copy number variation1nstd166human GRCh37.p13 chr20: 30,421,677-30,423,104 , GRCh38.p12 chr20: 31,833,874-31,835,301 MYLK2
    nsv3922338copy number variation1nstd102humanLikely pathogenic NCBI36 chr20: 29,297,047-30,068,749 , GRCh37 chr20: 29,833,386-30,605,088 , GRCh38 chr20: 31,245,583-32,017,285 BCL2L1, CD24P3, 38 more genes
    nsv3920371copy number variation1nstd102humanUncertain significance NCBI36 chr20: 28,266,169-30,026,184 , GRCh37.p13 chr20: 29,652,508-30,562,523 , GRCh38.p12 chr20: 30,417,832-31,974,720 LOC107985416, LOC110467523, 56 more genes
    nsv3920218copy number variation1nstd102humanPathogenic GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118 MIR3646, NPEPL1, 1310 more genes
    nsv3918053copy number variation1nstd102humanPathogenic NCBI36 chr20: 25,703,100-38,491,480 , GRCh37.p13 chr20: 25,755,100-39,058,066 , GRCh38.p12 chr20: 25,774,464-40,429,426 MYH7B, PPP1R16B, 300 more genes
    nsv3917138copy number variation1nstd102humanPathogenic GRCh38 chr20: 31,254,983-33,473,080 , NCBI36 chr20: 29,306,447-31,524,547 , GRCh37 chr20: 29,842,786-32,060,886 HAUS6P2, DEFB119, 78 more genes
    nsv3912259copy number variation1nstd102humanPathogenic GRCh38 chr20: 31,254,983-32,575,288 , NCBI36 chr20: 29,306,447-30,626,751 , GRCh37 chr20: 29,842,786-31,163,090 RNA5SP482, DKKL1P1, 51 more genes
    nsv3910818copy number variation1nstd102humanUncertain significance NCBI36 chr20: 25,616,026-62,435,964 , GRCh37.p13 chr20: 25,668,026-62,965,520 , GRCh38.p12 chr20: 25,687,390-64,334,167 RNA5SP481, LOC105372625, 855 more genes
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