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Variant : CV164826 (GRCh38/hg38 3p26.3(chr3:182931-937659)x3) Homo sapiens

Symbol: CV164826
Name: GRCh38/hg38 3p26.3(chr3:182931-937659)x3
Condition: See cases [RCV000143139]
Clinical Significance: likely benign|uncertain significance
Last Evaluated: 09/27/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CHL1   CHL1-AS1   CHL1-AS2   LINC01266  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000003.12:g.(?_182931)_(937659_?)dup
NC_000003.11:g.(?_224614)_(979343_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh383182,931 - 937,659CLINVAR
GRCh373224,614 - 979,343CLINVAR
Build 363199,614 - 954,343CLINVAR
Cytogenetic Map33p26.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9490737
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.