17716619 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv1058202	copy number variation	1	nstd100	human		NCBI36 chr21: 13,628,638-14,550,539 , GRCh37.p13 chr21: 14,706,767-15,628,668 , GRCh38.p12 chr21: 13,334,446-14,256,347	MIR3156-3, FEM1AP1, 38 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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