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Variant : CV157587 (NCBI36/hg18 14q32.33(chr14:105143707-105280567)x1) Homo sapiens

Symbol: CV157587
Name: NCBI36/hg18 14q32.33(chr14:105143707-105280567)x1
Condition: See cases [RCV000136963]
Clinical Significance: benign
Last Evaluated: 10/19/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: IGH   IGHA1   IGHG1   IGHG2   IGHG4   MIR8071-1   MIR8071-2  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NW_004166863.1:g.(?_269492)_(406352_?)del
NC_000014.7:g.(?_105143707)_(105280567_?)del
Position
Human AssemblyChrPosition (strand)Source
Build 3614105,143,707 - 105,280,567CLINVAR
Cytogenetic Map1414q32.33CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9484524
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-05-26
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.