25097466 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv1160441	copy number variation	1	nstd111	human		GRCh38.p12 chr16: 87,761,248-87,867,260 , GRCh37 chr16: 87,794,854-87,900,866	SLC7A5, KLHDC4, 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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