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Variant : CV601263 (GRCh37/hg19 7p15.3(chr7:23330347-23454296)x3) Homo sapiens

Symbol: CV601263
Name: GRCh37/hg19 7p15.3(chr7:23330347-23454296)x3
Condition: not provided [RCV000746563]
Clinical Significance: benign
Last Evaluated: 03/15/2011
Review Status: no assertion criteria provided
Related Genes: IGF2BP3   MALSU1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37723,330,347 - 23,454,296CLINVAR
Cytogenetic Map77p15.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14361920
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-01-14
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.