Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Variant : CV605850 (GRCh37/hg19 14q32.33(chr14:105943679-106190145)x1) Homo sapiens

Symbol: CV605850
Name: GRCh37/hg19 14q32.33(chr14:105943679-106190145)x1
Condition: not provided [RCV000751150]
Clinical Significance: benign
Last Evaluated: 09/23/2014
Review Status: no assertion criteria provided
Related Genes: CRIP1   CRIP2   IGH   IGHA1   IGHA2   IGHE   IGHG2   IGHG4   TEDC1   TMEM121  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3714105,943,679 - 106,190,145CLINVAR
Cytogenetic Map1414q32.33CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14366476
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-02-20
Status: ACTIVE



NHLBI Logo

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.