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Items: 1 to 20 of 192

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5954189copy number variation1nstd209human GRCh38 chr20: 32,061,191-32,062,146 , GRCh37.p13 chr20: 30,648,994-30,649,949 HCK
    nsv5540497insertion1nstd206human GRCh38 chr20: 32,061,233-32,061,233 , GRCh37.p13 chr20: 30,649,036-30,649,036 HCK
    nsv5532320copy number variation1nstd206human GRCh38 chr20: 32,061,142-32,062,094 , GRCh37.p13 chr20: 30,648,945-30,649,897 HCK
    nsv5518232copy number variation1nstd206human GRCh38 chr20: 32,061,000-32,066,100 , GRCh37.p13 chr20: 30,648,803-30,653,903 HCK
    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
    nsv5178037mobile element insertion1nstd203human GRCh38 chr20: 32,061,233-32,061,276 , GRCh37.p13 chr20: 30,649,036-30,649,079 HCK
    nsv5169360mobile element insertion1nstd203human GRCh38 chr20: 32,088,684-32,088,695 , GRCh37.p13 chr20: 30,676,487-30,676,498 HCK
    nsv5025511copy number variation1nstd200human GRCh38 chr20: 32,060,348-32,061,234 , GRCh37.p13 chr20: 30,648,151-30,649,037 HCK
    nsv5022324copy number variation1nstd200human GRCh38 chr20: 32,081,452-32,081,707 , GRCh37.p13 chr20: 30,669,255-30,669,510 HCK
    nsv4868576copy number variation1nstd200human GRCh37 chr20: 30,648,962-30,649,913 , GRCh38.p12 chr20: 32,061,159-32,062,110 HCK
    nsv4868575copy number variation1nstd200human GRCh37 chr20: 30,648,199-30,648,949 , GRCh38.p12 chr20: 32,060,396-32,061,146 HCK
    nsv4575117mobile element insertion1nstd166human GRCh37.p13 chr20: 30,687,083-30,687,083 , GRCh38.p12 chr20: 32,099,280-32,099,280 HCK
    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
    nsv4288459copy number variation1nstd166human GRCh37.p13 chr20: 30,651,179-30,654,346 , GRCh38.p12 chr20: 32,063,376-32,066,543 HCK
    nsv4273335copy number variation1nstd166human GRCh37.p13 chr20: 30,682,518-30,682,600 , GRCh38.p12 chr20: 32,094,715-32,094,797 HCK
    nsv3920503copy number variation1nstd102humanPathogenic GRCh38 chr20: 32,062,768-35,906,606 , NCBI36 chr20: 30,114,232-33,957,942 , GRCh37 chr20: 30,650,571-34,494,528 UQCC1, MIR1289-1, 111 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
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