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Variant : CV603399 (GRCh37/hg19 9q34.11-34.12(chr9:131413885-133866894)x1) Homo sapiens

Symbol: CV603399
Name: GRCh37/hg19 9q34.11-34.12(chr9:131413885-133866894)x1
Condition: not provided [RCV000748699]
Clinical Significance: benign
Last Evaluated: 06/27/2011
Review Status: no assertion criteria provided
Related Genes: ABL1   ASB6   ASS1   C9orf106   C9orf50   C9orf78   CRAT   DOLK   DOLPP1   ENDOG   EXOSC2   FIBCD1   FNBP1   FUBP3   GPR107   HMCN2   IER5L   KYAT1   LRRC8A   MIGA2   NCS1   NTMT1   NUP188   PHYHD1   PKN3   PRDM12   PRRX2   PTGES   PTPA   QRFP   SET   SH3GLB2   SPOUT1   TBC1D13   TOR1A   TOR1B   USP20   WDR34   ZDHHC12   ZER1  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh379131,413,885 - 133,866,894CLINVAR
Cytogenetic Map99q34.11-34.12CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14364032
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-02-11
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.