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Variant : CV554978 (GRCh37/hg19 10q26.13-26.3(chr10:127375792-135427143)x1) Homo sapiens

Symbol: CV554978
Name: GRCh37/hg19 10q26.13-26.3(chr10:127375792-135427143)x1
Condition: not provided [RCV000683283]
Clinical Significance: pathogenic
Last Evaluated: 08/03/2017
Review Status: no assertion criteria provided
Related Genes: ADAM12   ADAM8   ADGRA1   BCCIP   BNIP3   C10orf90   CALY   CFAP46   CLRN3   CYP2E1   DHX32   DOCK1   DPYSL4   EBF3   ECHS1   EDRF1   FANK1   FOXI2   FUOM   GLRX3   INPP5A   INSYN2A   JAKMIP3   KNDC1   LINC01166   LINC02870   LRRC27   MGMT   MKI67   MMP21   MTG1   NKX6-2   NPS   PAOX   PPP2R2D   PRAP1   PTPRE   PWWP2B   SPRN   STK32C   SYCE1   TCERG1L   TCERG1L-AS1   TUBGCP2   UROS   UTF1   VENTX   ZNF511  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3710127,375,792 - 135,427,143CLINVAR
Cytogenetic Map1010q26.13-26.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13796339
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2020-05-26
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.