50176204 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4634377	copy number variation	1	nstd184	human		GRCh37 chrX: 149,613,840-150,156,259 , GRCh38.p12 chrX: 150,445,574-150,987,786	HMGB3, MTM1, 6 more genes

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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.
Taxonomy
Link from dbVar to Taxonomy

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