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Variant : CV604697 (GRCh37/hg19 11p14.2-13(chr11:27154853-33302474)x1) Homo sapiens

Symbol: CV604697
Name: GRCh37/hg19 11p14.2-13(chr11:27154853-33302474)x1
Condition: not provided [RCV000749997]
Clinical Significance: pathogenic
Last Evaluated: 01/04/2011
Review Status: no assertion criteria provided
Related Genes: ARL14EP   BDNF   BDNF-AS   CCDC34   CCDC73   CSTF3   DCDC1   DEPDC7   DNAJC24   EIF3M   ELP4   FSHB   HIPK3   IMMP1L   KCNA4   KIF18A   LGR4   LIN7C   LINC00294   METTL15   MIR610   MPPED2   PAX6   PRRG4   QSER1   RCN1   TCP11L1   WT1   WT1-AS  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371127,154,853 - 33,302,474CLINVAR
Cytogenetic Map1111p14.2-13CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14365325
Created: 2019-02-12
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.