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Variant : CV382489 (GRCh37/hg19 9q21.12(chr9:72628750-73183334)x3) Homo sapiens

Symbol: CV382489
Name: GRCh37/hg19 9q21.12(chr9:72628750-73183334)x3
Condition: See cases [RCV000446264]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: KLF9   MAMDC2   SMC5   TRPM3  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37972,628,750 - 73,183,334CLINVAR
Cytogenetic Map99q21.12CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12850990
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-01-14
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.