17719193 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv1060776	copy number variation	1	nstd100	human		NCBI36 chr22: 30,199,892-30,230,359 , GRCh37.p13 chr22: 31,869,892-31,900,359 , GRCh38.p12 chr22: 31,473,906-31,504,373	RNU6-28P, SFI1, 1 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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