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Variant : CV154427 (GRCh38/hg38 8p23.3(chr8:241605-458761)x3) Homo sapiens

Symbol: CV154427
Name: GRCh38/hg38 8p23.3(chr8:241605-458761)x3
Condition: See cases [RCV000134118]
Clinical Significance: benign|likely benign|conflicting data from submitters
Last Evaluated: 09/21/2012
Review Status: classified by multiple submitters|classified by single submitter|no assertion criteria provided
Related Genes: FAM87A   FBXO25   ZNF596  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000008.11:g.(?_241605)_(458761_?)dup
NC_000008.10:g.(?_191605)_(408761_?)dup
NC_000008.9:g.(?_181605)_(398761_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh388241,605 - 458,761CLINVAR
GRCh378191,605 - 408,761CLINVAR
Build 368181,605 - 398,761CLINVAR
Cytogenetic Map88p23.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9489924
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-09-22
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.