878498 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv428361	copy number variation	6	nstd8	human		GRCh38.p12 chr19: 4,510,042-4,689,189 , GRCh37.p13 chr19: 4,510,054-4,689,201 , NCBI36 chr19: 4,461,054-4,640,201	SEMA6B, MYDGF, 8 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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