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Variant : CV554526 (GRCh37/hg19 7p22.3(chr7:2363275-2707822)x3) Homo sapiens

Symbol: CV554526
Name: GRCh37/hg19 7p22.3(chr7:2363275-2707822)x3
Condition: not provided [RCV000682831]
Clinical Significance: uncertain significance
Last Evaluated: 07/19/2017
Review Status: no assertion criteria provided
Related Genes: BRAT1   CHST12   EIF3B   IQCE   LFNG   TTYH3  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3772,363,275 - 2,707,822CLINVAR
Cytogenetic Map77p22.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13795765
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2020-03-24
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.