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Variant : CV160686 (GRCh38/hg38 14q32.33(chr14:106329896-106879298)x1) Homo sapiens

Symbol: CV160686
Name: GRCh38/hg38 14q32.33(chr14:106329896-106879298)x1
Condition: See cases [RCV000139727]
Clinical Significance: likely benign
Last Evaluated: 06/20/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: IGH   IGHV1-45   IGHV1-46   IGHV1-58   IGHV1-69   IGHV1-69-2   IGHV1-69D   IGHV2-70   IGHV2-70D   IGHV3-30   IGHV3-33   IGHV3-35   IGHV3-38   IGHV3-43   IGHV3-48   IGHV3-49   IGHV3-53   IGHV3-64   IGHV3-66   IGHV3-72   IGHV3-73   IGHV3-74   IGHV4-30-2   IGHV4-31   IGHV4-34   IGHV4-39   IGHV4-59   IGHV4-61   IGHV5-51   IGHV7-81   LINC00221   MIR5195  
Variant Type: copy number loss (SO:0001743)
Evidence: clinical testing
HGVS Name(s): NC_000014.9:g.(?_106329896)_(106879298_?)del
Human AssemblyChrPosition (strand)Source
GRCh3814106,329,896 - 106,879,298CLINVAR
GRCh3714106,786,148 - 107,287,505CLINVAR
Build 3614105,857,193 - 106,358,550CLINVAR
Cytogenetic Map1414q32.33CLINVAR

References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 9487257
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.