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Variant : CV602822 (GRCh37/hg19 9p24.2-21.3(chr9:4420767-22195820)x3) Homo sapiens

Symbol: CV602822
Name: GRCh37/hg19 9p24.2-21.3(chr9:4420767-22195820)x3
Condition: not provided [RCV000748122]
Clinical Significance: pathogenic
Last Evaluated: 01/14/2016
Review Status: no assertion criteria provided
Related Genes: ACER2   ADAMTSL1   AK3   BNC2   CCDC171   CD274   CDC37L1   CDKN2A   CDKN2B   CDKN2B-AS1   CER1   CNTLN   DENND4C   DMAC1   ERMP1   FOCAD   FREM1   GLDC   HACD4   HAUS6   IFNA1   IFNA10   IFNA13   IFNA14   IFNA16   IFNA17   IFNA2   IFNA21   IFNA4   IFNA5   IFNA6   IFNA7   IFNA8   IFNB1   IFNE   IFNW1   IL33   INSL4   INSL6   JAK2   KDM4C   KIAA2026   KLHL9   LURAP1L   MIR101-2   MIR31   MLANA   MLLT3   MPDZ   MTAP   NFIB   PDCD1LG2   PLGRKT   PLIN2   PLPP6   PSIP1   PTPRD   RANBP6   RCL1   RIC1   RLN1   RLN2   RPS6   RRAGA   SAXO1   SH3GL2   SLC1A1   SLC24A2   SNAPC3   SPATA6L   TPD52L3   TTC39B   TYRP1   UHRF2   ZDHHC21  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3794,420,767 - 22,195,820CLINVAR
Cytogenetic Map99p24.2-21.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14363455
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-01-21
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.