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Variant : CV156490 (GRCh38/hg38 14q32.33(chr14:106208348-106467748)x1) Homo sapiens

Symbol: CV156490
Name: GRCh38/hg38 14q32.33(chr14:106208348-106467748)x1
Condition: See cases [RCV000135985]
Clinical Significance: benign
Last Evaluated: 10/30/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: IGH   IGHV1-24   IGHV2-26   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 loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000014.9:g.(?_106208348)_(106467748_?)del
NC_000014.8:g.(?_106664991)_(106923671_?)del
NC_000014.7:g.(?_105736036)_(105994716_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh3814106,208,348 - 106,467,748CLINVAR
GRCh3714106,664,991 - 106,923,671CLINVAR
Build 3614105,736,036 - 105,994,716CLINVAR
Cytogenetic Map1414q32.33CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9483549
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.