48488155 - dbVar - NCBI

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Number of Variants: 1

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3924800	copy number variation	3	nstd102	human	Uncertain significance, Uncertain significance; Pathogenic/Likely pathogenic	GRCh37 chr16: 21,837,492-22,407,931 , NCBI36 chr16: 21,744,993-22,315,432 , GRCh38 chr16: 21,826,171-22,396,610	CDR2, UQCRC2, 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
Pathways + GO
Pathways, annotations and biological systems (BioSystems) that cite genes containing current variations.
Taxonomy
Link from dbVar to Taxonomy

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