4791778 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv834217	copy number variation	2	nstd68	human		NCBI35 chr22: 42,466,073-42,640,963 , GRCh37.p13 chr22: 44,141,172-44,316,062 , GRCh38.p12 chr22: 43,745,292-43,920,182	HMGN2P9, SULT4A1, 6 more genes

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