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

Variant : CV162750 (GRCh38/hg38 5p14.3(chr5:20474639-20673991)x1) Homo sapiens

Symbol: CV162750
Name: GRCh38/hg38 5p14.3(chr5:20474639-20673991)x1
Condition: See cases [RCV000141498]
Clinical Significance: benign
Last Evaluated: 02/04/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CDH18   LINC02146   LINC02241  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000005.10:g.(?_20474639)_(20673991_?)del
NC_000005.9:g.(?_20474748)_(20674100_?)del
NC_000005.8:g.(?_20510505)_(20709857_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38520,474,639 - 20,673,991CLINVAR
GRCh37520,474,748 - 20,674,100CLINVAR
Build 36520,510,505 - 20,709,857CLINVAR
Cytogenetic Map55p14.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9489023
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-02-11
Status: ACTIVE



NHLBI Logo

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