48457484 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3894129	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 73,023,062-73,524,207 , GRCh38.p12 chr7: 73,608,732-74,109,877	ELN-AS1, DNAJC30, 15 more genes

ClinVar
Clinical reports for this variation
Functional Class
Functional class of the sequence domain architecture
Gene
Link from dbVar to Gene
Pathways + GO
Pathways, annotations and biological systems (BioSystems) that cite genes containing current variations.
Taxonomy
Link from dbVar to Taxonomy

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