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Variant : CV159879 (GRCh38/hg38 15q21.1(chr15:44765914-45476854)x3) Homo sapiens

Symbol: CV159879
Name: GRCh38/hg38 15q21.1(chr15:44765914-45476854)x3
Condition: See cases [RCV000139024]
Clinical Significance: uncertain significance
Last Evaluated: 06/01/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AC051619.4   C15orf48   DUOX1   DUOX2   DUOXA1   DUOXA2   GATM   MIR147B   SHF   SLC28A2   SORD   SPATA5L1   TERB2   TRH-GTG1-7   TRH-GTG1-8   TRH-GTG1-9   TRIM69  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000015.10:g.(?_44765914)_(45476854_?)dup
NC_000015.9:g.(?_45058112)_(45769052_?)dup
NC_000015.8:g.(?_42845404)_(43556344_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381544,765,914 - 45,476,854CLINVAR
GRCh371545,058,112 - 45,769,052CLINVAR
Build 361542,845,404 - 43,556,344CLINVAR
Cytogenetic Map1515q21.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9486556
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-08-04
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.