25097586 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv1160561	copy number variation	1	nstd111	human		GRCh38.p12 chr19: 1,884,553-2,003,982 , GRCh37 chr19: 1,884,552-2,003,981	CSNK1G2, BTBD2, 5 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

nsv1160561 (1)
dbVar
GEO Profile Links for Gene (Select 728537) (737)
GEO Profiles
GEO Profile Links for PMC (Select 32086) (96)
GEO Profiles
Homo sapiens chromosome 2 open reading frame 92 (C2orf92), transcript variant 1,...
Homo sapiens chromosome 2 open reading frame 92 (C2orf92), transcript variant 1, mRNA
gi|1890346221|ref|NM_001351368.2|

Nucleotide
PREDICTED: Homo sapiens chromosome 2 open reading frame 92 (C2orf92), transcript...
PREDICTED: Homo sapiens chromosome 2 open reading frame 92 (C2orf92), transcript variant X5, mRNA
gi|2217330691|ref|XM_024453111.2|

Nucleotide

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