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Variant : CV556191 (GRCh37/hg19 22q11.22-11.23(chr22:22953514-23654007)x3) Homo sapiens

Symbol: CV556191
Name: GRCh37/hg19 22q11.22-11.23(chr22:22953514-23654007)x3
Condition: not provided [RCV000684482]
Clinical Significance: uncertain significance
Last Evaluated: 08/08/2017
Review Status: no assertion criteria provided
Related Genes: BCR   GGTLC2   GNAZ   IGLC1   IGLL5   RAB36   RSPH14  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372222,953,514 - 23,654,007CLINVAR
Cytogenetic Map2222q11.22-11.23CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13798718
Created: 2018-10-09
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.