48450620 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3887265	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr12: 100,886,254-100,917,988 , GRCh38 chr12: 100,492,476-100,524,210	NR1H4

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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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