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Variant : CV157122 (GRCh38/hg38 9p23(chr9:10126221-12031786)x3) Homo sapiens

Symbol: CV157122
Name: GRCh38/hg38 9p23(chr9:10126221-12031786)x3
Condition: See cases [RCV000136569]
Clinical Significance: 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.(?_10126221)_(12031786_?)dup
NC_000009.11:g.(?_10126221)_(12031786_?)dup
NC_000009.10:g.(?_10116221)_(12021786_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38910,126,221 - 12,031,786CLINVAR
GRCh37910,126,221 - 12,031,786CLINVAR
Build 36910,116,221 - 12,021,786CLINVAR
Cytogenetic Map99p23CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9484130
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-06-30
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.