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Variant : CV553949 (GRCh37/hg19 3p22.2(chr3:38021661-38510752)x3) Homo sapiens

Symbol: CV553949
Name: GRCh37/hg19 3p22.2(chr3:38021661-38510752)x3
Condition: not provided [RCV000682254]
Clinical Significance: uncertain significance
Last Evaluated: 07/25/2017
Review Status: no assertion criteria provided
Related Genes: ACAA1   ACVR2B   CTDSPL   DLEC1   MYD88   OXSR1   PLCD1   SLC22A13   SLC22A14   VILL   XYLB  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37338,021,661 - 38,510,752CLINVAR
Cytogenetic Map33p22.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13795031
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2020-01-21
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.