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Variant : CV381131 (GRCh37/hg19 9p21.3(chr9:20951885-22447709)x1) Homo sapiens

Symbol: CV381131
Name: GRCh37/hg19 9p21.3(chr9:20951885-22447709)x1
Condition: See cases [RCV000448195]
Clinical Significance: pathogenic
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: CDKN2A   CDKN2B   CDKN2B-AS1   DMRTA1   FOCAD   HACD4   IFNA1   IFNA10   IFNA13   IFNA14   IFNA16   IFNA17   IFNA2   IFNA21   IFNA4   IFNA5   IFNA6   IFNA7   IFNA8   IFNB1   IFNE   IFNW1   KLHL9   MIR31   MTAP  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37920,951,885 - 22,447,709CLINVAR
Cytogenetic Map99p21.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12852905
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-03-31
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.