25097207 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv1160182	copy number variation	1	nstd111	human		GRCh38.p12 chr1: 17,655,418-18,282,385 , GRCh37 chr1: 17,981,913-18,608,879	ARHGEF10L, ACTL8, 6 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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