11818502 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
esv2716966	copy number variation	35	estd201	human		GRCh37 chr18: 34,917,892-34,918,708 , GRCh38.p12 chr18: 37,337,929-37,338,745	CELF4

Functional Class
Functional class of the sequence domain architecture
Gene
Link from dbVar to Gene
Pathways + GO
Pathways, annotations and biological systems (BioSystems) that cite genes containing current variations.
PubMed
Link from dbVar to PubMed
Taxonomy
Link from dbVar to Taxonomy

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