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Variant : CV672137 (Single allele) Homo sapiens

Symbol: CV672137
Name: Single allele
Condition: not provided [RCV000844961]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided
Related Genes: ACP5   ANGPTL8   AP1M2   ATG4D   C19orf38   CARM1   CCDC151   CCDC159   CDKN2D   CNN1   DHPS   DNM2   DOCK6   ECSIT   ELAVL3   ELOF1   EPOR   FBXW9   ILF3   KANK2   KRI1   LDLR   MAN2B1   MIR199A1   PRKCSH   QTRT1   RAB3D   RGL3   SLC44A2   SMARCA4   SPC24   SWSAP1   TIMM29   TMED1   TMEM205   TNPO2   TSPAN16   WDR83   WDR83OS   YIPF2   ZNF136   ZNF20   ZNF433   ZNF439   ZNF44   ZNF440   ZNF441   ZNF442   ZNF443   ZNF490   ZNF491   ZNF563   ZNF564   ZNF625   ZNF627   ZNF653   ZNF69   ZNF700   ZNF709   ZNF763   ZNF791   ZNF799   ZNF823   ZNF844   ZNF878  
Variant Type: deletion (SO:0000159)
Source: CLINVAR
Evidence: phenotyping only
Position
Human AssemblyChrPosition (strand)Source
GRCh371910,642,984 - 12,810,067CLINVAR
Cytogenetic Map1919p13.2CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14746763
Created: 2019-09-06
Species: Homo sapiens
Last Modified: 2019-11-12
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.