48474791 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3911436	copy number variation	2	nstd102	human	Pathogenic	GRCh38 chr7: 73,192,369-74,779,057 , GRCh37 chr7: 72,606,409-74,193,403 , NCBI36 chr7: 72,244,345-73,831,339	0

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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