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Variant : CV164932 (GRCh38/hg38 8p23.3(chr8:226452-1670285)x1) Homo sapiens

Symbol: CV164932
Name: GRCh38/hg38 8p23.3(chr8:226452-1670285)x1
Condition: See cases [RCV000143245]
Clinical Significance: uncertain significance
Last Evaluated: 12/10/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AC100797.4   AF067845.2   DLGAP2   DLGAP2-AS1   ERICH1   FAM87A   FBXO25   LOC105377777   TDRP   ZNF596  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000008.11:g.(?_226452)_(1670285_?)del
NC_000008.10:g.(?_176452)_(1618451_?)del
NC_000008.9:g.(?_166452)_(1605858_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh388226,452 - 1,670,285CLINVAR
GRCh378176,452 - 1,618,451CLINVAR
Build 368166,452 - 1,605,858CLINVAR
Cytogenetic Map88p23.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9490843
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-09-22
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.