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

Variant : CV160679 (GRCh38/hg38 7q11.21(chr7:65017875-65835330)x1) Homo sapiens

Symbol: CV160679
Name: GRCh38/hg38 7q11.21(chr7:65017875-65835330)x1
Condition: See cases [RCV000139720]
Clinical Significance: likely benign
Last Evaluated: 10/10/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: LOC441242   SNORA15B-1   SNORA15B-2   SNORA22   SNORA22C   ZNF92  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000007.14:g.(?_65017875)_(65835330_?)del
NC_000007.13:g.(?_64478253)_(65300317_?)del
NC_000007.12:g.(?_64115688)_(64937752_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38765,017,875 - 65,835,330CLINVAR
GRCh37764,478,253 - 65,300,317CLINVAR
Build 36764,115,688 - 64,937,752CLINVAR
Cytogenetic Map77q11.21CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9487250
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-01-14
Status: ACTIVE



NHLBI Logo

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