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Variant : CV165030 (GRCh38/hg38 5p14.3(chr5:19857588-20747237)x3) Homo sapiens

Symbol: CV165030
Name: GRCh38/hg38 5p14.3(chr5:19857588-20747237)x3
Condition: See cases [RCV000143343]
Clinical Significance: uncertain significance
Last Evaluated: 10/23/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CDH18   CDH18-AS1   LINC02146   LINC02241  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000005.10:g.(?_19857588)_(20747237_?)dup
NC_000005.9:g.(?_19857697)_(20747346_?)dup
NC_000005.8:g.(?_19893454)_(20783103_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38519,857,588 - 20,747,237CLINVAR
GRCh37519,857,697 - 20,747,346CLINVAR
Build 36519,893,454 - 20,783,103CLINVAR
Cytogenetic Map55p14.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9490941
Created: 2014-09-09
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.