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

Variant : CV553998 (GRCh37/hg19 3q21.1-21.2(chr3:122698091-125036994)x1) Homo sapiens

Symbol: CV553998
Name: GRCh37/hg19 3q21.1-21.2(chr3:122698091-125036994)x1
Condition: not provided [RCV000682303]
Clinical Significance: uncertain significance
Last Evaluated: 10/20/2017
Review Status: no assertion criteria provided
Related Genes: ADCY5   CCDC14   HACD2   HEG1   ITGB5   KALRN   MUC13   MYLK   PDIA5   ROPN1   SEC22A   SEMA5B   SLC12A8   UMPS   ZNF148  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh373122,698,091 - 125,036,994CLINVAR
Cytogenetic Map33q21.1-21.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13795080
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2019-11-12
Status: ACTIVE



NHLBI Logo

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