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Variant : CV435403 (GRCh37/hg19 22q13.31(chr22:44382852-45007914)x1) Homo sapiens

Symbol: CV435403
Name: GRCh37/hg19 22q13.31(chr22:44382852-45007914)x1
Condition: See cases [RCV000511840]
Clinical Significance: uncertain significance
Last Evaluated: 09/09/2015
Review Status: no assertion criteria provided
Related Genes: PARVB   PARVG   RTL6   SAMM50   SHISAL1  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372244,382,852 - 45,007,914CLINVAR
Cytogenetic Map2222q13.31CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13444809
Created: 2017-11-07
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.