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Variant : CV436186 (GRCh37/hg19 8p21.1-12(chr8:27501662-29342607)x3) Homo sapiens

Symbol: CV436186
Name: GRCh37/hg19 8p21.1-12(chr8:27501662-29342607)x3
Condition: See cases [RCV000510519]
Clinical Significance: uncertain significance
Last Evaluated: 03/16/2015
Review Status: no assertion criteria provided
Related Genes: CCDC25   DUSP4   ELP3   ESCO2   EXTL3   FBXO16   FZD3   HMBOX1   INTS9   KIF13B   NUGGC   PBK   PNOC   SCARA3   SCARA5   ZNF395  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37827,501,662 - 29,342,607CLINVAR
Cytogenetic Map88p21.1-12CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13443498
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-06-23
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.