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

Variant : CV158413 (GRCh38/hg38 7q11.23(chr7:73286412-73556222)x1) Homo sapiens

Symbol: CV158413
Name: GRCh38/hg38 7q11.23(chr7:73286412-73556222)x1
Condition: See cases [RCV000137730]
Clinical Significance: uncertain significance
Last Evaluated: 08/29/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: BAZ1B   BCL7B   FKBP6   FZD9   NSUN5   TRIM50  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000007.14:g.(?_73286412)_(73556222_?)del
NC_000007.12:g.(?_72338350)_(72608488_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38773,286,412 - 73,556,222CLINVAR
Build 36772,338,350 - 72,608,488CLINVAR
Cytogenetic Map77q11.23CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9485282
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-01-21
Status: ACTIVE



NHLBI Logo

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