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Variant : CV383049 (GRCh37/hg19 3q21.2-21.3(chr3:124806350-126567150)x4) Homo sapiens

Symbol: CV383049
Name: GRCh37/hg19 3q21.2-21.3(chr3:124806350-126567150)x4
Condition: See cases [RCV000448957]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: ALDH1L1   ALG1L   C3orf22   CFAP100   CHCHD6   CHST13   KLF15   OSBPL11   ROPN1B   SLC12A8   SLC41A3   SNX4   TXNRD3   UROC1   ZNF148   ZXDC  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh373124,806,350 - 126,567,150CLINVAR
Cytogenetic Map33q21.2-21.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12853657
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.