17721229 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv1062812	copy number variation	1	nstd100	human		NCBI36 chr19: 49,734,102-49,906,636 , GRCh37.p13 chr19: 45,042,262-45,214,796 , GRCh38.p12 chr19: 44,538,275-44,711,525	CEACAM19, CEACAM16-AS1, 6 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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