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Variant : CV596478 (GRCh37/hg19 22q11.21(chr22:21679616-22095920)x1) Homo sapiens

Symbol: CV596478
Name: GRCh37/hg19 22q11.21(chr22:21679616-22095920)x1
Condition: not provided [RCV000741778]
Clinical Significance: benign
Last Evaluated: 01/24/2011
Review Status: no assertion criteria provided
Related Genes: CCDC116   HIC2   MIR130B   PPIL2   RIMBP3B   RIMBP3C   SDF2L1   TMEM191C   UBE2L3   YDJC   YPEL1  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372221,679,616 - 22,095,920CLINVAR
Cytogenetic Map2222q11.21CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14357152
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-11-05
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.