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Variant : CV435274 (GRCh37/hg19 11p14.1-12(chr11:27588560-41770792)x1) Homo sapiens

Symbol: CV435274
Name: GRCh37/hg19 11p14.1-12(chr11:27588560-41770792)x1
Condition: See cases [RCV000511434]
Clinical Significance: pathogenic|uncertain significance
Last Evaluated: 02/14/2018
Review Status: no assertion criteria provided
Related Genes: ABTB2   APIP   ARL14EP   BDNF   BDNF-AS   C11orf91   CAPRIN1   CAT   CCDC73   CD44   CD59   COMMD9   CSTF3   DCDC1   DEPDC7   DNAJC24   EHF   EIF3M   ELF5   ELP4   FBXO3   FJX1   FSHB   HIPK3   IFTAP   IMMP1L   KCNA4   KIAA1549L   KIF18A   LDLRAD3   LINC00294   LMO2   LRRC4C   METTL15   MIR610   MPPED2   NAT10   PAMR1   PAX6   PDHX   PRR5L   PRRG4   QSER1   RAG1   RAG2   RCN1   SLC1A2   TCP11L1   TRAF6   TRIM44   WT1   WT1-AS  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371127,588,560 - 41,770,792CLINVAR
Cytogenetic Map1111p14.1-12CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13444406
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-02-11
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.