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Variant : CV157084 (GRCh38/hg38 9p23(chr9:10425554-11318889)x3) Homo sapiens

Symbol: CV157084
Name: GRCh38/hg38 9p23(chr9:10425554-11318889)x3
Condition: See cases [RCV000136538]
Clinical Significance: likely benign|uncertain significance
Last Evaluated: 12/22/2010
Review Status: classified by 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.(?_10425554)_(11318889_?)dup
NC_000009.11:g.(?_10425554)_(11318889_?)dup
NC_000009.10:g.(?_10415554)_(11308889_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38910,425,554 - 11,318,889CLINVAR
GRCh37910,425,554 - 11,318,889CLINVAR
Build 36910,415,554 - 11,308,889CLINVAR
Cytogenetic Map99p23CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9484099
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-06-23
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.