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Variant : CV601394 (GRCh37/hg19 7p12.2(chr7:49994609-50094083)x3) Homo sapiens

Symbol: CV601394
Name: GRCh37/hg19 7p12.2(chr7:49994609-50094083)x3
Condition: not provided [RCV000746694]
Clinical Significance: benign
Last Evaluated: 12/05/2013
Review Status: no assertion criteria provided
Related Genes: ZPBP  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37749,994,609 - 50,094,083CLINVAR
Cytogenetic Map77p12.2CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14362049
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-02-11
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.