25010313 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv1118758	copy number variation	1	nstd106	human		GRCh37 chr17: 40,830,900-40,831,500 , GRCh38.p12 chr17: 42,678,882-42,679,482	CNTNAP1, CCR10

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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