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Variant : CV157668 (GRCh38/hg38 14q32.33(chr14:106259748-106668563)x3) Homo sapiens

Symbol: CV157668
Name: GRCh38/hg38 14q32.33(chr14:106259748-106668563)x3
Condition: See cases [RCV000137031]
Clinical Significance: benign
Last Evaluated: 10/19/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: IGH   IGHV1-24   IGHV1-45   IGHV1-46   IGHV1-58   IGHV2-26   IGHV3-23   IGHV3-30   IGHV3-33   IGHV3-35   IGHV3-38   IGHV3-43   IGHV3-48   IGHV3-49   IGHV3-53   IGHV3-64   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)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000014.9:g.(?_106259748)_(106668563_?)dup
NC_000014.8:g.(?_106716345)_(107124579_?)dup
NC_000014.7:g.(?_105787390)_(106195624_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh3814106,259,748 - 106,668,563CLINVAR
GRCh3714106,716,345 - 107,124,579CLINVAR
Build 3614105,787,390 - 106,195,624CLINVAR
Cytogenetic Map1414q32.33CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9484591
Created: 2014-09-09
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.