48444130 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3880775	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 73,442,119-73,484,237 , GRCh38.p12 chr7: 74,027,789-74,069,907	0

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.
Taxonomy
Link from dbVar to Taxonomy

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