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Variant : CV607943 (GRCh37/hg19 9q34.3(chr9:140094273-140332474)x3) Homo sapiens

Symbol: CV607943
Name: GRCh37/hg19 9q34.3(chr9:140094273-140332474)x3
Condition: not provided [RCV000753243]
Clinical Significance: benign
Last Evaluated: 03/11/2013
Review Status: no assertion criteria provided
Related Genes: CYSRT1   ENTPD8   EXD3   FAM166A   NDOR1   NELFB   NOXA1   NRARP   RNF208   RNF224   SLC34A3   STPG3   TMEM203   TOR4A   TPRN   TUBB4B  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh379140,094,273 - 140,332,474CLINVAR
Cytogenetic Map99q34.3CLINVAR

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 14349863
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-01-14
Status: ACTIVE


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