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Variant : CV382672 (GRCh37/hg19 10q26.12-26.3(chr10:122343861-135427143)x1) Homo sapiens

Symbol: CV382672
Name: GRCh37/hg19 10q26.12-26.3(chr10:122343861-135427143)x1
Condition: See cases [RCV000446095]
Clinical Significance: pathogenic
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: ABRAXAS2   ACADSB   ADAM12   ADAM8   ADGRA1   ARMS2   ATE1   BCCIP   BNIP3   BTBD16   BUB3   C10orf120   C10orf88   C10orf90   CALY   CFAP46   CHST15   CLRN3   CPXM2   CTBP2   CUZD1   CYP2E1   DHX32   DMBT1   DOCK1   DPYSL4   EBF3   ECHS1   EDRF1   EEF1AKMT2   FAM24A   FAM24B   FAM53B   FANK1   FGFR2   FOXI2   FUOM   GLRX3   GPR26   HMX2   HMX3   HTRA1   IKZF5   INPP5A   INSYN2A   JAKMIP3   KNDC1   LHPP   LINC01166   LINC02870   LRRC27   MGMT   MKI67   MMP21   MTG1   NKX1-2   NKX6-2   NPS   NSMCE4A   OAT   PAOX   PLEKHA1   PLPP4   PPP2R2D   PRAP1   PSTK   PTPRE   PWWP2B   SPRN   STK32C   SYCE1   TACC2   TCERG1L   TCERG1L-AS1   TEX36   TUBGCP2   UROS   UTF1   VENTX   WDR11   ZNF511   ZRANB1  
Variant Type: copy number loss (SO:0001743)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh3710122,343,861 - 135,427,143CLINVAR
Cytogenetic Map1010q26.12-26.3CLINVAR

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 12850823
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-08-04
Status: ACTIVE


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