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Variant : CV436770 (GRCh37/hg19 10q26.3(chr10:134593406-135427143)x1) Homo sapiens

Symbol: CV436770
Name: GRCh37/hg19 10q26.3(chr10:134593406-135427143)x1
Condition: See cases [RCV000510608]
Clinical Significance: uncertain significance
Last Evaluated: 01/05/2015
Review Status: no assertion criteria provided
Related Genes: ADAM8   ADGRA1   CALY   CFAP46   CYP2E1   ECHS1   FUOM   INPP5A   KNDC1   LINC01166   MTG1   NKX6-2   PAOX   PRAP1   SPRN   SYCE1   TUBGCP2   UTF1   VENTX   ZNF511  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3710134,593,406 - 135,427,143CLINVAR
Cytogenetic Map1010q26.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13443587
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-05-19
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.