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Variant : CV673034 (GRCh37/hg19 7p12.1-11.1(chr7:52809787-58025873)x1) Homo sapiens

Symbol: CV673034
Name: GRCh37/hg19 7p12.1-11.1(chr7:52809787-58025873)x1
Condition: not provided [RCV000846150]
Clinical Significance: uncertain significance
Last Evaluated: 04/04/2018
Review Status: no assertion criteria provided
Related Genes: CCT6A   CHCHD2   EGFR   LANCL2   MRPS17   NIPSNAP2   NUPR2   PHKG1   POM121L12   PSPH   SEC61G   SEPTIN14   SUMF2   VOPP1   VSTM2A   ZNF479   ZNF713   ZNF716  
Variant Type: copy number loss (SO:0001743)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh37752,809,787 - 58,025,873CLINVAR
Cytogenetic Map77p12.1-11.1CLINVAR

Additional Information

External Database Links
RGD Object Information
RGD ID: 14976718
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-05-12
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.