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Variant : CV436206 (GRCh37/hg19 3q21.2-21.3(chr3:124990032-126088215)x3) Homo sapiens

Symbol: CV436206
Name: GRCh37/hg19 3q21.2-21.3(chr3:124990032-126088215)x3
Condition: See cases [RCV000510692]
Clinical Significance: uncertain significance
Last Evaluated: 08/13/2015
Review Status: no assertion criteria provided
Related Genes: ALDH1L1   ALG1L   KLF15   OSBPL11   ROPN1B   SLC41A3   SNX4   ZNF148  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh373124,990,032 - 126,088,215CLINVAR
Cytogenetic Map33q21.2-21.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13443671
Created: 2017-11-07
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.