25097755 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv1160730	copy number variation	1	nstd111	human		GRCh37 chr22: 21,728,138-21,988,019 , GRCh38.p12 chr22: 21,373,849-21,633,730	UBE2L3, HIC2, 9 more genes

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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