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Variant : CV164050 (GRCh38/hg38 9p23(chr9:9972107-12031786)x1) Homo sapiens

Symbol: CV164050
Name: GRCh38/hg38 9p23(chr9:9972107-12031786)x1
Condition: See cases [RCV000142367]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: PTPRD   PTPRD-AS2  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000009.12:g.(?_9972107)_(12031786_?)del
NC_000009.11:g.(?_9972107)_(12031786_?)del
NC_000009.10:g.(?_9962107)_(12021786_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh3899,972,107 - 12,031,786CLINVAR
GRCh3799,972,107 - 12,031,786CLINVAR
Build 3699,962,107 - 12,021,786CLINVAR
Cytogenetic Map99p23CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9489886
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-07-07
Status: ACTIVE



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