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Variant : CV157957 (GRCh38/hg38 9p23(chr9:10006230-11086155)x1) Homo sapiens

Symbol: CV157957
Name: GRCh38/hg38 9p23(chr9:10006230-11086155)x1
Condition: See cases [RCV000137281]
Clinical Significance: uncertain significance
Last Evaluated: 03/21/2011
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.(?_10006230)_(11086155_?)del
NC_000009.11:g.(?_10006230)_(11086155_?)del
NC_000009.10:g.(?_9996230)_(11076155_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38910,006,230 - 11,086,155CLINVAR
GRCh37910,006,230 - 11,086,155CLINVAR
Build 3699,996,230 - 11,076,155CLINVAR
Cytogenetic Map99p23CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9484838
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.