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Variant : CV157579 (GRCh38/hg38 14q32.33(chr14:106112755-106714110)x3) Homo sapiens

Symbol: CV157579
Name: GRCh38/hg38 14q32.33(chr14:106112755-106714110)x3
Condition: See cases [RCV000136956]
Clinical Significance: benign
Last Evaluated: 10/19/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: IGH   IGHV1-18   IGHV1-24   IGHV1-45   IGHV1-46   IGHV1-58   IGHV2-26   IGHV3-11   IGHV3-13   IGHV3-15   IGHV3-16   IGHV3-20   IGHV3-21   IGHV3-23   IGHV3-30   IGHV3-33   IGHV3-35   IGHV3-38   IGHV3-43   IGHV3-48   IGHV3-49   IGHV3-53   IGHV3-64   IGHV3-66   IGHV4-28   IGHV4-30-2   IGHV4-31   IGHV4-34   IGHV4-39   IGHV4-59   IGHV4-61   IGHV5-51   LINC00221   LINC00226  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
HGVS Name(s): NC_000014.9:g.(?_106112755)_(106714110_?)dup
Human AssemblyChrPosition (strand)Source
GRCh3814106,112,755 - 106,714,110CLINVAR
GRCh3714106,538,421 - 107,169,357CLINVAR
Build 3614105,609,466 - 106,240,402CLINVAR
Cytogenetic Map1414q32.33CLINVAR

References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 9484517
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-07-28
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.