17802233 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
esv3575445	copy number variation	1	estd212	human		GRCh37 chr22: 24,171,305-24,271,732 , GRCh38.p12 chr22: 23,829,118-23,929,545 , GRCh38.p12 chr22\|NT_187633.1: 65,480-165,907	MIF, SMARCB1, 6 more genes

Functional Class
Functional class of the sequence domain architecture
Gene
Link from dbVar to Gene
GEO DataSets
Link from dbVar to GEO DataSets
Nucleotide
Link from dbVar to Nucleotide
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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