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

Variant : CV153975 (GRCh38/hg38 8p23.1(chr8:11901356-12610034)x1) Homo sapiens

Symbol: CV153975
Name: GRCh38/hg38 8p23.1(chr8:11901356-12610034)x1
Condition: See cases [RCV000133706]
Clinical Significance: benign
Last Evaluated: 05/27/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AC068587.4   DEFB130A   DEFB130B   DEFB134   DEFB135   DEFB136   FAM66A   FAM66D   FAM85A   FAM86B1   FAM86B2   USP17L2   USP17L7   ZNF705D  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000008.11:g.(?_11901356)_(12610034_?)del
NC_000008.10:g.(?_11758865)_(12467543_?)del
NC_000008.9:g.(?_11796274)_(12511914_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38811,901,356 - 12,610,034CLINVAR
GRCh37811,758,865 - 12,467,543CLINVAR
Build 36811,796,274 - 12,511,914CLINVAR
Cytogenetic Map88p23.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9481291
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-06-23
Status: ACTIVE



NHLBI Logo

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