48448197 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3884842	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 75,600,108-76,063,285 , GRCh38.p12 chr15: 75,307,767-75,770,944	DNM1P35, NEIL1, 17 more genes

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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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