7-0067-003 AND nstd173 - dbVar - NCBI

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

Search results

Items: 13

loading data ...

Number of Variants: 13

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4387639	copy number variation	1	nstd173	human		GRCh37 chr7: 141,755,372-141,804,540 , GRCh38.p12 chr7: 142,055,572-142,104,740 , GRCh38.p12 chr7\|NT_187562.1: 17,452-66,620	MGAM
nsv4370897	copy number variation	108	nstd173	human		GRCh37 chr13: 57,758,269-57,778,367 , GRCh38.p12 chr13: 57,184,135-57,204,233	MTCO2P3
nsv4365971	copy number variation	432	nstd173	human		GRCh37 chr1: 248,753,196-248,795,289 , GRCh38.p12 chr1: 248,589,895-248,631,988	OR2T10, OR2T11
nsv4368298	copy number variation	45	nstd173	human		GRCh37 chrX: 62,432,151-62,505,606 , GRCh38.p12 chrX: 63,212,272-63,285,729	LOC100533730, LOC105377212
nsv4385330	copy number variation	98	nstd173	human		GRCh37 chr6: 257,340-294,826 , GRCh38.p12 chr6: 257,340-294,826	, , 1 more genes
nsv4378692	copy number variation	10	nstd173	human		GRCh37 chr14: 106,890,795-106,918,056 , GRCh38.p12 chr14: 106,434,885-106,462,131 , GRCh38.p12 chr14\|NT_187600.1: 926,564-953,810	IGHV3-41, IGHVII-40-1, 3 more genes
nsv4382082	copy number variation	609	nstd173	human		GRCh37 chr11: 55,374,019-55,442,305 , GRCh38.p12 chr11: 55,606,543-55,674,829	OR4C6, OR4P4, 2 more genes
nsv4380451	copy number variation	20	nstd173	human		GRCh37 chr12: 11,215,480-11,251,705 , GRCh38.p12 chr12: 11,062,881-11,099,106	TAS2R64P, TAS2R43, 3 more genes
nsv4381644	copy number variation	30	nstd173	human		GRCh37 chr5: 27,606,792-27,632,299 , GRCh38.p12 chr5: 27,606,685-27,632,192	0
nsv4383204	copy number variation	1	nstd173	human		GRCh37 chrX: 1,734,398-2,127,589 , GRCh38.p12 chrX: 1,615,505-2,209,570	, , 5 more genes
nsv4369116	copy number variation	1	nstd173	human		GRCh37 chr11: 119,362,673-119,590,889 , GRCh38.p12 chr11: 119,491,961-119,720,179	NECTIN1, KRT8P7, 5 more genes
nsv4375926	copy number variation	10	nstd173	human		GRCh37 chr19: 20,829,413-20,997,330 , GRCh38.p12 chr19: 20,646,607-20,814,524 , GRCh38.p12 chr19\|NW_003315962.1: 1-151,498	ZNF66, LOC105372319, 4 more genes
nsv4366569	copy number variation	1	nstd173	human		GRCh37 chrX: 4,668,449-4,958,582 , GRCh38.p12 chrX: 4,750,408-5,040,541	0

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

7-0067-003 AND nstd173 (14)
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)