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Items: 1 to 20 of 178

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976704inversion1nstd209human GRCh38 chr20: 36,955,252-45,585,469 , GRCh37.p13 chr20: 35,583,655-44,214,108 , ADA, 180 more genes
    nsv5593761copy number variation1nstd207human GRCh38 chr20: 37,572,226-37,572,276 , GRCh37.p13 chr20: 36,200,628-36,200,678 LINC01746
    nsv5526447copy number variation1nstd206human GRCh38 chr20: 37,571,678-37,575,450 , GRCh37.p13 chr20: 36,200,080-36,203,852 LINC01746
    nsv5514246copy number variation1nstd206human GRCh38 chr20: 37,575,282-37,576,465 , GRCh37.p13 chr20: 36,203,684-36,204,867 LINC01746
    nsv5324090inversion1nstd204human GRCh37.p13 chr20: 35,583,652-44,214,109 , GRCh38.p13 chr20: 36,955,249-45,585,470 , BPI, 180 more genes
    nsv5033948inversion1nstd200human GRCh38 chr20: 36,955,253-45,585,464 , GRCh37.p13 chr20: 35,583,656-44,214,103 , EMILIN3, 180 more genes
    nsv5028541copy number variation1nstd200human GRCh38 chr20: 37,575,496-37,576,554 , GRCh37.p13 chr20: 36,203,898-36,204,956 LINC01746
    nsv5028540copy number variation1nstd200human GRCh38 chr20: 37,566,776-37,569,587 , GRCh37.p13 chr20: 36,195,178-36,197,989 LINC01746
    nsv5022343copy number variation1nstd200human GRCh38 chr20: 32,602,560-45,347,064 , GRCh37.p13 chr20: 31,190,362-43,975,704 , SNHG11, 286 more genes
    nsv5022342copy number variation1nstd200human GRCh38 chr20: 32,576,247-46,538,786 , GRCh37.p13 chr20: 31,164,049-45,167,425 , NECAB3, 350 more genes
    nsv5022326copy number variation1nstd200human GRCh38 chr20: 32,216,214-44,981,731 , GRCh37.p13 chr20: 30,804,017-43,610,372 , HNF4A, 279 more genes
    nsv4884257inversion1nstd200human GRCh37 chr20: 35,583,656-44,214,103 , GRCh38.p12 chr20: 36,955,253-45,585,464 , TGM2, 180 more genes
    nsv4868593copy number variation1nstd200human GRCh37 chr20: 31,164,049-45,167,425 , GRCh38.p12 chr20: 32,576,247-46,538,786 , MMP24-AS1-EDEM2, 350 more genes
    nsv4868578copy number variation1nstd200human GRCh37 chr20: 30,804,017-43,610,372 , GRCh38.p12 chr20: 32,216,214-44,981,731 , SNORA71C, 279 more genes
    nsv4749887copy number variation1nstd199human GRCh37 chr20: 36,200,586-36,200,646 , GRCh38.p12 chr20: 37,572,184-37,572,244 LINC01746
    nsv4679317copy number variation1nstd189human GRCh37.p13 chr20: 36,043,180-36,348,971 , GRCh38.p12 chr20: 37,414,777-37,720,569 NNAT, BLCAP, 8 more genes
    nsv4674805copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 34,980,430-46,806,549 , GRCh38.p12 chr20: 36,352,027-48,177,806 ADA, BPI, 266 more genes
    nsv4630305copy number variation1nstd183human GRCh37 chr20: 36,199,998-36,203,870 , GRCh38.p12 chr20: 37,571,596-37,575,468 LINC01746
    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
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