dbVar for OMIM (Select 194190) - dbVar

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

Links from OMIM

loading data ...

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7098818	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 11,399,082-38,137,335 , GRCh37.p13 chr4: 11,400,706-38,138,956	LOC105374542, PPARGC1A, 232 more genes
nsv4347802	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 75,742-8,672,411 , GRCh38.p12 chr4: 75,849-8,670,685	RNA5SP152, LOC101928306, 200 more genes
nsv4347791	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 19,186,845-24,548,281 , GRCh38.p12 chr4: 19,185,222-24,546,658	PACRGL, LOC105374528, 29 more genes
nsv4347682	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 1,305,802-2,460,571 , GRCh38.p12 chr4: 1,312,014-2,458,844	NSD2, SPICP5, 29 more genes
nsv997085	copy number variation	1	nstd45	human	Pathogenic	GRCh38.p12 chr4: 337,779-2,009,235 , GRCh37 chr4: 331,568-2,010,962	, ATP5ME, 58 more genes