53209127 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6137725	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr22: 23,774,226-23,859,697 , GRCh37.p13 chr22: 24,116,413-24,201,884	SMARCB1, MMP11, 2 more genes

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ClinVar
Clinical reports for this variation
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.
Taxonomy
Link from dbVar to Taxonomy

dbVar for OMIM (Select 614608) (2)
dbVar
Assembly for Nucleotide (Select 2431560057) (1)
Assembly
Metagenome-assembled genome: SRR9217414_bin.59_CONCOCT_v1.1_MAG
Metagenome-assembled genome: SRR9217414_bin.59_CONCOCT_v1.1_MAG

biosample
Homo sapiens high-mobility group 20B, mRNA (cDNA clone MGC:32098 IMAGE:4873122),...
Homo sapiens high-mobility group 20B, mRNA (cDNA clone MGC:32098 IMAGE:4873122), complete cds
gi|18204332|gb|BC021585.1|

Nucleotide

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