48434492 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3871137	copy number variation	4	nstd102	human	Pathogenic	GRCh38 chr2: 110,123,336-110,205,062 , GRCh37 chr2: 110,880,913-110,962,639	ACTR1AP1, NPHP1

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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.
PubMed
Link from dbVar to PubMed
Taxonomy
Link from dbVar to Taxonomy

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