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Variant : CV674967 (GRCh37/hg19 22q11.22-11.23(chr22:22962196-23652512)x1) Homo sapiens

Symbol: CV674967
Name: GRCh37/hg19 22q11.22-11.23(chr22:22962196-23652512)x1
Condition: not provided [RCV000848074]
Clinical Significance: pathogenic
Last Evaluated: 05/05/2017
Review Status: no assertion criteria provided
Related Genes: BCR   GGTLC2   GNAZ   IGLC1   IGLL5   RAB36   RSPH14  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372222,962,196 - 23,652,512CLINVAR
Cytogenetic Map2222q11.22-11.23CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14976521
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-09-08
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.