49342383 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4347470	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 190,039,387-190,040,504 , GRCh38.p12 chr3: 190,321,598-190,322,715	CLDN1, CLDN16

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ClinVar
Clinical reports for this variation
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.
Taxonomy
Link from dbVar to Taxonomy

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