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Variant : CV436843 (GRCh37/hg19 7p13(chr7:44688036-45364793)x3) Homo sapiens

Symbol: CV436843
Name: GRCh37/hg19 7p13(chr7:44688036-45364793)x3
Condition: See cases [RCV000511814]
Clinical Significance: likely benign
Last Evaluated: 12/16/2014
Review Status: no assertion criteria provided
Related Genes: CCM2   H2AZ2   MYO1G   NACAD   OGDH   PPIA   PURB   RAMP3   SNHG15   SNORA5C   TBRG4   ZMIZ2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37744,688,036 - 45,364,793CLINVAR
Cytogenetic Map77p13CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13444783
Created: 2017-11-07
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.