47178759 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3319005	copy number variation	1	nstd45	human	Pathogenic	GRCh38.p12 chr22: 42,160,013-42,283,927 , GRCh37 chr22: 42,556,019-42,679,933	TCF20, OGFRP1

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BioProjects
Link from dbVar to BioProjects
Functional Class
Functional class of the sequence domain architecture
Gene
Link from dbVar to Gene
OMIM
Link from dbVar to OMIM
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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