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Variant : CV383016 (GRCh37/hg19 22q13.31(chr22:45769244-46630634)x1) Homo sapiens

Symbol: CV383016
Name: GRCh37/hg19 22q13.31(chr22:45769244-46630634)x1
Condition: See cases [RCV000446891]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: ATXN10   FBLN1   MIRLET7A3   MIRLET7B   PPARA   PRR34   RIBC2   SMC1B   WNT7B  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372245,769,244 - 46,630,634CLINVAR
Cytogenetic Map2222q13.31CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 12851613
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-09-22
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.