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Variant : CV382380 (GRCh37/hg19 13q34(chr13:111058488-111317455)x3) Homo sapiens

Symbol: CV382380
Name: GRCh37/hg19 13q34(chr13:111058488-111317455)x3
Condition: See cases [RCV000445721]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: CARS2   COL4A2   NAXD   RAB20  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3713111,058,488 - 111,317,455CLINVAR
Cytogenetic Map1313q34CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12850455
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2019-11-12
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.