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Variant : CV161365 (GRCh38/hg38 6q13(chr6:70309182-70479207)x3) Homo sapiens

Symbol: CV161365
Name: GRCh38/hg38 6q13(chr6:70309182-70479207)x3
Condition: See cases [RCV000140318]
Clinical Significance: uncertain significance
Last Evaluated: 04/30/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: EVADR   FAM135A   FAM135A-AS1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000006.12:g.(?_70309182)_(70479207_?)dup
NC_000006.11:g.(?_71018885)_(71188910_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38670,309,182 - 70,479,207CLINVAR
GRCh37671,018,885 - 71,188,910CLINVAR
Build 36671,075,606 - 71,245,631CLINVAR
Cytogenetic Map66q13CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9487848
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-09-22
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.