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Variant : CV158063 (GRCh38/hg38 7p12.3(chr7:48734588-48997715)x1) Homo sapiens

Symbol: CV158063
Name: GRCh38/hg38 7p12.3(chr7:48734588-48997715)x1
Condition: See cases [RCV000137387]
Clinical Significance: uncertain significance
Last Evaluated: 02/08/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CDC14C  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000007.14:g.(?_48734588)_(48997715_?)del
NC_000007.13:g.(?_48774184)_(49037311_?)del
NC_000007.12:g.(?_48744730)_(49007857_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38748,734,588 - 48,997,715CLINVAR
GRCh37748,774,184 - 49,037,311CLINVAR
Build 36748,744,730 - 49,007,857CLINVAR
Cytogenetic Map77p12.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9484944
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-05-12
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.