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Variant : CV555315 (GRCh37/hg19 14q32.33(chr14:106020225-107285437)x1) Homo sapiens

Symbol: CV555315
Name: GRCh37/hg19 14q32.33(chr14:106020225-107285437)x1
Condition: not provided [RCV000683620]
Clinical Significance: likely benign
Last Evaluated: 03/21/2018
Review Status: no assertion criteria provided
Related Genes: IGH   IGHA1   IGHA2   IGHD   IGHD3-3   IGHE   IGHG1   IGHG2   IGHG3   IGHG4   IGHM   IGHV3-23  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3714106,020,225 - 107,285,437CLINVAR
Cytogenetic Map1414q32.33CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13797195
Created: 2018-10-09
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.