17716398 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv1057981	copy number variation	1	nstd100	human		NCBI36 chr21: 41,584,092-41,716,628 , GRCh37.p13 chr21: 42,662,222-42,794,758 , GRCh38.p12 chr21: 41,290,295-41,422,831	FAM3B, MX2, 1 more genes

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.
PubMed
Link from dbVar to PubMed
Taxonomy
Link from dbVar to Taxonomy

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