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Variant : CV673578 (GRCh37/hg19 14q32.33(chr14:105677530-106044679)x3) Homo sapiens

Symbol: CV673578
Name: GRCh37/hg19 14q32.33(chr14:105677530-106044679)x3
Condition: not provided [RCV000846694]
Clinical Significance: uncertain significance
Last Evaluated: 12/12/2017
Review Status: no assertion criteria provided
Related Genes: BRF1   BTBD6   CRIP1   CRIP2   IGH   MTA1   PACS2   TEDC1   TEX22   TMEM121  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh3714105,677,530 - 106,044,679CLINVAR
Cytogenetic Map1414q32.33CLINVAR

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 14977267
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-02-11
Status: ACTIVE


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