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Variant : CV155149 (GRCh38/hg38 6q26(chr6:162232971-162708613)x3) Homo sapiens

Symbol: CV155149
Name: GRCh38/hg38 6q26(chr6:162232971-162708613)x3
Condition: See cases [RCV000134782]
Clinical Significance: uncertain significance
Last Evaluated: 08/30/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: PRKN  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000006.12:g.(?_162232971)_(162708613_?)dup
NC_000006.11:g.(?_162654003)_(163129645_?)dup
NC_000006.10:g.(?_162573993)_(163049635_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh386162,232,971 - 162,708,613CLINVAR
GRCh376162,654,003 - 163,129,645CLINVAR
Build 366162,573,993 - 163,049,635CLINVAR
Cytogenetic Map66q26CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9482359
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-12-03
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.