4791799 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv834238	copy number variation	2	nstd68	human		NCBI35 chr22: 49,131,263-49,285,538 , GRCh37.p13 chr22: 50,841,119-50,995,394 , GRCh38.p12 chr22: 50,402,690-50,556,965	TYMP, SBF1, 13 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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