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Variant : CV435539 (GRCh37/hg19 2q22.3(chr2:144796786-145564689)x1) Homo sapiens

Symbol: CV435539
Name: GRCh37/hg19 2q22.3(chr2:144796786-145564689)x1
Condition: See cases [RCV000510654]
Clinical Significance: pathogenic
Last Evaluated: 06/16/2014
Review Status: no assertion criteria provided
Related Genes: GTDC1   ZEB2  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372144,796,786 - 145,564,689CLINVAR
Cytogenetic Map22q22.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13443633
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2019-12-03
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.