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Variant : CV161752 (GRCh38/hg38 8q24.3(chr8:144468986-144535245)x3) Homo sapiens

Symbol: CV161752
Name: GRCh38/hg38 8q24.3(chr8:144468986-144535245)x3
Condition: See cases [RCV000140675]
Clinical Significance: benign
Last Evaluated: 04/30/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ARHGAP39   C8orf82   FOXH1   GPT   KIFC2   LRRC14   LRRC24   MFSD3   PPP1R16A   RECQL4  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000008.11:g.(?_144468986)_(144535245_?)dup
NC_000008.10:g.(?_145694369)_(145760629_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh388144,468,986 - 144,535,245CLINVAR
GRCh378145,694,369 - 145,760,629CLINVAR
Build 368145,665,177 - 145,731,437CLINVAR
Cytogenetic Map88q24.3CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9488205
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-03-24
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.