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Variant : CV436349 (GRCh37/hg19 9q21.11-21.31(chr9:68734571-83557267)x3) Homo sapiens

Symbol: CV436349
Name: GRCh37/hg19 9q21.11-21.31(chr9:68734571-83557267)x3
Condition: See cases [RCV000510725]
Clinical Significance: pathogenic
Last Evaluated: 02/29/2016
Review Status: no assertion criteria provided
Related Genes: ABHD17B   ALDH1A1   ANXA1   APBA1   BANCR   C9orf135   C9orf40   C9orf57   C9orf85   CARNMT1   CARNMT1-AS1   CBWD3   CBWD5   CBWD6   CEMIP2   CEP78   FAM122A   FAM189A2   FOXB2   FOXD4L3   FOXD4L4   FOXD4L5   FOXD4L6   FXN   GCNT1   GDA   GNA14   GNAQ   KLF9   MAMDC2   MIR204   NMRK1   OSTF1   PCA3   PCSK5   PGM5   PIP5K1B   PRKACG   PRUNE2   PSAT1   PTAR1   RFK   RORB   SMC5   TJP2   TLE4   TMC1   TMEM252   TRPM3   TRPM6   VPS13A   ZFAND5  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh37968,734,571 - 83,557,267CLINVAR
Cytogenetic Map99q21.11-21.31CLINVAR

References - uncurated

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 13443703
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-01-07
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.