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Variant : CV596725 (GRCh37/hg19 22q13.31(chr22:44564975-44569346)x1) Homo sapiens

Symbol: CV596725
Name: GRCh37/hg19 22q13.31(chr22:44564975-44569346)x1
Condition: not provided [RCV000742025]
Clinical Significance: benign
Last Evaluated: 12/14/2012
Review Status: no assertion criteria provided
Related Genes: PARVB   PARVG  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372244,564,975 - 44,569,346CLINVAR
Cytogenetic Map2222q13.31CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14357399
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-09-29
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.