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Variant : CV436620 (GRCh37/hg19 10q26.3(chr10:134615768-135184126)x3) Homo sapiens

Symbol: CV436620
Name: GRCh37/hg19 10q26.3(chr10:134615768-135184126)x3
Condition: See cases [RCV000512163]
Clinical Significance: likely benign
Last Evaluated: 08/22/2014
Review Status: no assertion criteria provided
Related Genes: ADAM8   ADGRA1   CALY   CFAP46   ECHS1   FUOM   KNDC1   LINC01166   PRAP1   TUBGCP2   UTF1   VENTX   ZNF511  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3710134,615,768 - 135,184,126CLINVAR
Cytogenetic Map1010q26.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13445130
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.