17692181 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv1033764	copy number variation	1	nstd100	human		NCBI36 chr9: 13,754,918-14,216,168 , GRCh37.p13 chr9: 13,764,918-14,226,168 , GRCh38.p12 chr9: 13,764,919-14,226,169	PES1P2, NFIB, 5 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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