24501141 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv1067925	copy number variation	328	nstd104	human		GRCh37 chrY: 2,694,521-59,034,049 , GRCh38.p12 chrY: 2,826,480-56,887,902	ACTG1P2, AMELY, 525 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.
PubMed
Link from dbVar to PubMed
Taxonomy
Link from dbVar to Taxonomy

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