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Variant : CV160296 (GRCh38/hg38 14q32.33(chr14:106118296-106467900)x3) Homo sapiens

Symbol: CV160296
Name: GRCh38/hg38 14q32.33(chr14:106118296-106467900)x3
Condition: See cases [RCV000139385]
Clinical Significance: benign
Last Evaluated: 09/21/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: IGH   IGHV1-18   IGHV1-24   IGHV2-26   IGHV3-13   IGHV3-15   IGHV3-16   IGHV3-20   IGHV3-21   IGHV3-23   IGHV3-30   IGHV3-33   IGHV3-35   IGHV3-38   IGHV4-28   IGHV4-30-2   IGHV4-31   IGHV4-34   IGHV4-39   LINC00226  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000014.9:g.(?_106118296)_(106467900_?)dup
NC_000014.8:g.(?_106574892)_(106923823_?)dup
NC_000014.7:g.(?_105645937)_(105994868_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh3814106,118,296 - 106,467,900CLINVAR
GRCh3714106,574,892 - 106,923,823CLINVAR
Build 3614105,645,937 - 105,994,868CLINVAR
Cytogenetic Map1414q32.33CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9486916
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-08-04
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.