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Variant : CV157386 (GRCh38/hg38 14q32.33(chr14:105491009-105530212)x3) Homo sapiens

Symbol: CV157386
Name: GRCh38/hg38 14q32.33(chr14:105491009-105530212)x3
Condition: See cases [RCV000136798]
Clinical Significance: benign
Last Evaluated: 10/01/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: TEDC1   TMEM121  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000014.9:g.(?_105491009)_(105530212_?)dup
NW_004166863.1:g.(?_154176)_(193379_?)dup
NC_000014.7:g.(?_105028391)_(105067594_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh3814105,491,009 - 105,530,212CLINVAR
Build 3614105,028,391 - 105,067,594CLINVAR
Cytogenetic Map1414q32.33CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9484359
Created: 2014-09-09
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.