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Items: 1 to 20 of 134

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7019999copy number variation1nstd229human GRCh38 chr20: 35,486,342-36,114,422 , GRCh37.p13 chr20: 34,074,168-34,702,344 HMGB3P2, NFS1, 24 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
    nsv6521942copy number variation1nstd223human GRCh38 chr20: 35,789,861-35,966,037 , GRCh37.p13 chr20: 34,377,783-34,553,959 CNBD2, HIGD1AP16, 5 more genes
    nsv6146396copy number variation1nstd206human GRCh38 chr20: 35,928,297-35,928,349 , GRCh37.p13 chr20: 34,516,219-34,516,271 PHF20, RNU6-937P
    nsv6134023copy number variation1nstd213human GRCh37 chr20: 34,270,000-35,840,001 , GRCh38.p12 chr20: 35,682,078-37,211,598 RBL1, AAR2, 35 more genes
    nsv5668088insertion1nstd207human GRCh38 chr20: 35,928,297-35,928,297 , GRCh37.p13 chr20: 34,516,219-34,516,219 PHF20, RNU6-937P
    nsv5557509sequence alteration1nstd206human GRCh38 chr20: 35,627,992-36,077,048 , GRCh37.p13 chr20: 34,215,914-34,664,970 CPNE1, PHF20, 16 more genes
    nsv5025549copy number variation1nstd200human GRCh38 chr20: 35,789,861-35,966,040 , GRCh37.p13 chr20: 34,377,783-34,553,962 COX7BP2, CNBD2, 5 more genes
    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
    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
    nsv4560081insertion1nstd166human GRCh37.p13 chr20: 34,516,219-34,516,219 , GRCh38.p12 chr20: 35,928,297-35,928,297 PHF20, RNU6-937P
    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
    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
    nsv3913594copy number variation1nstd102humanPathogenic GRCh37 chr20: 32,020,169-35,450,284 , NCBI36 chr20: 31,483,830-34,883,698 , GRCh38 chr20: 33,432,363-36,821,881 AHCY, RALY, 93 more genes
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