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Variant : CV156024 (GRCh38/hg38 6q13(chr6:70809191-71941709)x3) Homo sapiens

Symbol: CV156024
Name: GRCh38/hg38 6q13(chr6:70809191-71941709)x3
Condition: See cases [RCV000135579]
Clinical Significance: uncertain significance
Last Evaluated: 01/27/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: B3GAT2   LINC00472   LINC01626   MIR30A   MIR30C2   OGFRL1   RIMS1   SMAP1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000006.12:g.(?_70809191)_(71941709_?)dup
NC_000006.11:g.(?_71518894)_(72651412_?)dup
NC_000006.10:g.(?_71575615)_(72708133_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38670,809,191 - 71,941,709CLINVAR
GRCh37671,518,894 - 72,651,412CLINVAR
Build 36671,575,615 - 72,708,133CLINVAR
Cytogenetic Map66q13CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9483151
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-06-30
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.