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Variant : CV165241 (GRCh38/hg38 10q26.3(chr10:130625650-133613639)x1) Homo sapiens

Symbol: CV165241
Name: GRCh38/hg38 10q26.3(chr10:130625650-133613639)x1
Condition: See cases [RCV000143554]
Clinical Significance: uncertain significance
Last Evaluated: 08/19/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ADAM8   ADGRA1   ADGRA1-AS1   BNIP3   CALY   CFAP46   CYP2E1   DPYSL4   ECHS1   FUOM   INPP5A   JAKMIP3   KNDC1   LINC01164   LINC01165   LINC01166   LINC01167   LINC01168   LINC02870   LRRC27   MIR202   MIR202HG   MIR378C   MIR3944   MTG1   NKX6-2   PAOX   PPP2R2D   PRAP1   PWWP2B   SPRN   STK32C   SYCE1   TCERG1L   TCERG1L-AS1   TUBGCP2   UTF1   VENTX   ZNF511  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000010.11:g.(?_130625650)_(133613639_?)del
NC_000010.10:g.(?_132423914)_(135427143_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh3810130,625,650 - 133,613,639CLINVAR
GRCh3710132,423,914 - 135,427,143CLINVAR
Build 3610132,313,904 - 135,277,133CLINVAR
Cytogenetic Map1010q26.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9491152
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-02-20
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.