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

Variant : CV163659 (GRCh38/hg38 7q35(chr7:143728625-144176869)x1) Homo sapiens

Symbol: CV163659
Name: GRCh38/hg38 7q35(chr7:143728625-144176869)x1
Condition: See cases [RCV000142117]
Clinical Significance: conflicting data from submitters
Last Evaluated:
Review Status: classified by multiple submitters|classified by single submitter|no assertion criteria provided
Related Genes: CTAGE6   OR2A12   OR2A14   OR2A2   OR2A25   OR2A5   OR2F1   OR2F2   OR6B1   TCAF1   TCAF2  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000007.14:g.(?_143728625)_(144176869_?)del
NC_000007.13:g.(?_143425718)_(143873962_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh387143,728,625 - 144,176,869CLINVAR
GRCh377143,425,718 - 143,873,962CLINVAR
Build 367143,056,651 - 143,504,895CLINVAR
Cytogenetic Map77q35CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9489986
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-02-20
Status: ACTIVE



NHLBI Logo

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