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Variant : CV74436 (GRCh38/hg38 14q32.33(chr14:106714051-106855263)x1) Homo sapiens

Symbol: CV74436
Name: GRCh38/hg38 14q32.33(chr14:106714051-106855263)x1
Condition: See cases [RCV000053709]
Clinical Significance: benign
Last Evaluated: 08/12/2011
Review Status: classified by single submitter|criteria provided, single submitter|no assertion criteria provided
Related Genes: IGH   IGHV1-69   IGHV1-69-2   IGHV1-69D   IGHV2-70   IGHV2-70D   IGHV3-72   IGHV3-73   IGHV3-74   MIR5195  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000014.9:g.(?_106714051)_(106855263_?)del
NC_000014.8:g.(?_107169298)_(107263478_?)del
NC_000014.7:g.(?_106240343)_(106334523_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh3814106,714,051 - 106,855,263CLINVAR
GRCh3714107,169,298 - 107,263,478CLINVAR
Build 3614106,240,343 - 106,334,523CLINVAR
Cytogenetic Map1414q32.33CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 8620627
Created: 2014-05-13
Species: Homo sapiens
Last Modified: 2020-07-28
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.