dbVar for OMIM (Select 608323) - dbVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Links from OMIM

Items: 4

loading data ...

Number of Variants: 4

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4682965	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 33,276,182-33,276,668 , GRCh38.p12 chr1: 32,810,581-32,811,067	YARS1
nsv4682512	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 33,241,572-33,263,454 , GRCh38.p12 chr1: 32,775,971-32,797,853	YARS1
nsv3888014	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr1: 32,810,591-32,811,057 , GRCh37 chr1: 33,276,192-33,276,658	YARS1
nsv3878135	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 33,241,563-46,663,513 , GRCh38.p12 chr1: 32,775,962-46,197,841	LINC02786, LOC105378678, 365 more genes

Supplemental Content

Filters: Manage Filters

Find related data

Recent activity

Clear Turn Off Turn On

dbVar for OMIM (Select 608323) (5)
dbVar

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)