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Variant : CV164799 (GRCh38/hg38 4p16.3(chr4:3407550-3942201)x1) Homo sapiens

Symbol: CV164799
Name: GRCh38/hg38 4p16.3(chr4:3407550-3942201)x1
Condition: See cases [RCV000143112]
Clinical Significance: uncertain significance
Last Evaluated: 03/19/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ADRA2C   DOK7   HGFAC   LINC00955   LINC02171   LRPAP1   RGS12  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000004.12:g.(?_3407550)_(3942201_?)del
NC_000004.11:g.(?_3409277)_(3943928_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh3843,407,550 - 3,942,201CLINVAR
GRCh3743,409,277 - 3,943,928CLINVAR
Build 3643,379,075 - 3,994,858CLINVAR
Cytogenetic Map44p16.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9490710
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-09-08
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.