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Variant : CV71785 (GRCh38/hg38 14q32.33(chr14:105939848-106451054)x1) Homo sapiens

Symbol: CV71785
Name: GRCh38/hg38 14q32.33(chr14:105939848-106451054)x1
Condition: See cases [RCV000050844]
Clinical Significance: benign
Last Evaluated: 08/12/2011
Review Status: classified by single submitter|criteria provided, single submitter|no assertion criteria provided
Related Genes: IGH   IGHV1-18   IGHV1-2   IGHV1-24   IGHV1-3   IGHV2-26   IGHV2-5   IGHV3-11   IGHV3-13   IGHV3-15   IGHV3-16   IGHV3-20   IGHV3-21   IGHV3-23   IGHV3-30   IGHV3-33   IGHV3-35   IGHV3-38   IGHV3-64D   IGHV3-7   IGHV4-28   IGHV4-30-2   IGHV4-31   IGHV4-34   IGHV4-39   IGHV4-4   IGHV5-10-1   IGHV6-1   IGHV7-4-1   LINC00226  
Variant Type: copy number loss (SO:0001743)
Evidence: clinical testing
HGVS Name(s): NC_000014.9:g.(?_105939848)_(106451054_?)del
Human AssemblyChrPosition (strand)Source
GRCh3814105,939,848 - 106,451,054CLINVAR
GRCh3714106,405,703 - 106,906,960CLINVAR
Build 3614105,476,748 - 105,978,005CLINVAR
Cytogenetic Map1414q32.33CLINVAR

References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 8617914
Created: 2014-05-13
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.