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

Variant : CV554408 (GRCh37/hg19 6q22.1(chr6:116656963-116903944)x3) Homo sapiens

Symbol: CV554408
Name: GRCh37/hg19 6q22.1(chr6:116656963-116903944)x3
Condition: not provided [RCV000682713]
Clinical Significance: uncertain significance
Last Evaluated: 03/21/2018
Review Status: no assertion criteria provided
Related Genes: CALHM4   CALHM5   CALHM6   DSE   RWDD1   TRAPPC3L  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh376116,656,963 - 116,903,944CLINVAR
Cytogenetic Map66q22.1CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13795582
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2020-07-07
Status: ACTIVE



NHLBI Logo

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