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Variant : CV673023 (GRCh37/hg19 5q11.2(chr5:56283070-58079028)x1) Homo sapiens

Symbol: CV673023
Name: GRCh37/hg19 5q11.2(chr5:56283070-58079028)x1
Condition: not provided [RCV000846139]
Clinical Significance: uncertain significance
Last Evaluated: 09/22/2017
Review Status: no assertion criteria provided
Related Genes: ACTBL2   GAPT   GPBP1   PLK2   RAB3C  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37556,283,070 - 58,079,028CLINVAR
Cytogenetic Map55q11.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14976706
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-01-07
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.