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

Variant : CV73060 (GRCh38/hg38 9p23(chr9:10381123-11173149)x3) Homo sapiens

Symbol: CV73060
Name: GRCh38/hg38 9p23(chr9:10381123-11173149)x3
Condition: See cases [RCV000052220]
Clinical Significance: uncertain significance
Last Evaluated: 08/12/2011
Review Status: classified by single submitter|criteria provided, single submitter|no assertion criteria provided
Related Genes: PTPRD   PTPRD-AS2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000009.12:g.(?_10381123)_(11173149_?)dup
NC_000009.11:g.(?_10381123)_(11173149_?)dup
NC_000009.10:g.(?_10371123)_(11163149_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38910,381,123 - 11,173,149CLINVAR
GRCh37910,381,123 - 11,173,149CLINVAR
Build 36910,371,123 - 11,163,149CLINVAR
Cytogenetic Map99p23CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 8619223
Created: 2014-05-13
Species: Homo sapiens
Last Modified: 2020-07-07
Status: ACTIVE



NHLBI Logo

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