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Variant : CV673430 (GRCh37/hg19 4q26(chr4:114579245-115640604)x3) Homo sapiens

Symbol: CV673430
Name: GRCh37/hg19 4q26(chr4:114579245-115640604)x3
Condition: not provided [RCV000846546]
Clinical Significance: uncertain significance
Last Evaluated: 03/06/2018
Review Status: no assertion criteria provided
Related Genes: ARSJ   CAMK2D   UGT8  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh374114,579,245 - 115,640,604CLINVAR
Cytogenetic Map44q26CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14977112
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-01-14
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.