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Variant : CV553835 (GRCh37/hg19 2q12.1-12.2(chr2:104327052-106123901)x3) Homo sapiens

Symbol: CV553835
Name: GRCh37/hg19 2q12.1-12.2(chr2:104327052-106123901)x3
Condition: not provided [RCV000682140]
Clinical Significance: uncertain significance
Last Evaluated: 04/20/2018
Review Status: no assertion criteria provided
Related Genes: C2orf49   FHL2   GPR45   MRPS9   POU3F3   TGFBRAP1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372104,327,052 - 106,123,901CLINVAR
Cytogenetic Map22q12.1-12.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13794913
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2020-03-24
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.