25006981 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv1115426	copy number variation	1	nstd106	human		GRCh37 chr12: 21,434,400-21,440,600 , GRCh38.p12 chr12: 21,281,466-21,287,666	SLCO1A2

BioProjects
Link from dbVar to BioProjects
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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