50286842 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4684017	copy number variation	142	nstd187	human		GRCh37 chr8: 6,872,895-6,876,338 , GRCh38.p12 chr8: 7,015,373-7,018,816 , GRCh38.p12 chr8\|NW_018654717.1: 410,494-413,940	DEFA3

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BioSample
Link from dbVar to BioSample
Functional Class
Functional class of the sequence domain architecture
Gene
Link from dbVar to Gene
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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