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Variant : CV603371 (GRCh37/hg19 9q33.3-34.12(chr9:129370440-133866894)x1) Homo sapiens

Symbol: CV603371
Name: GRCh37/hg19 9q33.3-34.12(chr9:129370440-133866894)x1
Condition: not provided [RCV000748671]
Clinical Significance: pathogenic
Last Evaluated: 06/27/2011
Review Status: no assertion criteria provided
Related Genes: ABL1   AK1   ANGPTL2   ASB6   ASS1   C9orf106   C9orf16   C9orf50   C9orf78   CDK9   CERCAM   CFAP157   CIZ1   COQ4   CRAT   DNM1   DOLK   DOLPP1   DPM2   ENDOG   ENG   EXOSC2   FAM102A   FIBCD1   FNBP1   FPGS   FUBP3   GARNL3   GLE1   GOLGA2   GPR107   HMCN2   IER5L   KYAT1   LCN2   LMX1B   LRRC8A   LRSAM1   MIGA2   MIR199B   MIR2861   NAIF1   NCS1   NIBAN2   NTMT1   NUP188   ODF2   PHYHD1   PIP5KL1   PKN3   PRDM12   PRRX2   PTGES   PTGES2   PTPA   PTRH1   QRFP   RALGPS1   RPL12   SET   SH2D3C   SH3GLB2   SLC25A25   SLC27A4   SLC2A8   SPOUT1   SPTAN1   ST6GALNAC4   ST6GALNAC6   STXBP1   SWI5   TBC1D13   TOR1A   TOR1B   TOR2A   TRUB2   TTC16   URM1   USP20   WDR34   ZBTB34   ZBTB43   ZDHHC12   ZER1   ZNF79  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh379129,370,440 - 133,866,894CLINVAR
Cytogenetic Map99q33.3-34.12CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14364004
Created: 2019-02-12
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.