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Variant : CV154042 (GRCh38/hg38 8p23.3(chr8:241530-451413)x3) Homo sapiens

Symbol: CV154042
Name: GRCh38/hg38 8p23.3(chr8:241530-451413)x3
Condition: See cases [RCV000133773]
Clinical Significance: uncertain significance
Last Evaluated: 02/28/2010
Review Status: 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.(?_241530)_(451413_?)dup
NC_000008.10:g.(?_191530)_(401413_?)dup
NC_000008.9:g.(?_181530)_(391413_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh388241,530 - 451,413CLINVAR
GRCh378191,530 - 401,413CLINVAR
Build 368181,530 - 391,413CLINVAR
Cytogenetic Map88p23.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9481358
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.