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Variant : CV381825 (GRCh37/hg19 1p35.3(chr1:28891341-28939710)x3) Homo sapiens

Symbol: CV381825
Name: GRCh37/hg19 1p35.3(chr1:28891341-28939710)x3
Condition: See cases [RCV000446159]
Clinical Significance: likely benign
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: RAB42   TAF12   TRNAU1AP  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37128,891,341 - 28,939,710CLINVAR
Cytogenetic Map11p35.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12850886
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-02-11
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.