52011638 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv5564215	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 90,870,713-90,871,071 , GRCh38.p12 chr14: 90,404,369-90,404,727	CALM1

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ClinVar
Clinical reports for this variation
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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