1-1049-003 AND nstd173 - dbVar - NCBI

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

Search results

Items: 18

loading data ...

Number of Variants: 18

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4383593	copy number variation	15	nstd173	human		GRCh37 chr3: 46,801,804-46,849,588 , GRCh38.p12 chr3: 46,760,314-46,808,098	PRSS44P
nsv4379109	copy number variation	1337	nstd173	human		GRCh37 chr20: 1,560,774-1,597,997 , GRCh38.p12 chr20: 1,580,128-1,617,351	SIRPB1
nsv4365093	copy number variation	508	nstd173	human		GRCh37 chr13: 57,758,269-57,778,379 , GRCh38.p12 chr13: 57,184,135-57,204,245	MTCO2P3
nsv4376456	copy number variation	1782	nstd173	human		GRCh37 chr8: 39,246,772-39,386,964 , GRCh38.p12 chr8: 39,389,253-39,529,445	ADAM5, ADAM3A
nsv4376403	copy number variation	119	nstd173	human		GRCh37 chr19: 53,517,242-53,553,087 , GRCh38.p12 chr19: 53,013,989-53,049,834	ERVV-1, ERVV-2
nsv4367018	copy number variation	2	nstd173	human		GRCh37 chrX: 119,028,443-119,057,536 , GRCh38.p12 chrX: 119,894,480-119,923,573	NKAP, AKAP14
nsv4365112	copy number variation	2	nstd173	human		GRCh37 chr1: 104,109,341-104,132,506 , GRCh38.p12 chr1: 103,566,719-103,589,884	AMY2B, ACTG1P4
nsv4379656	copy number variation	1	nstd173	human		GRCh37 chr6: 252,503-381,137 , GRCh38.p12 chr6: 252,503-381,137	DUSP22, , 1 more genes
nsv4385952	copy number variation	6	nstd173	human		GRCh37 chr14: 21,349,608-21,421,088 , GRCh38.p12 chr14: 20,881,449-20,952,929	RNASE3, LOC100507513, 1 more genes
nsv4383082	copy number variation	1	nstd173	human		GRCh37 chr4: 407,072-433,228 , GRCh38.p12 chr4: 413,283-439,439	ZNF721, LOC100533734, 1 more genes
nsv4381505	copy number variation	106	nstd173	human		GRCh37 chr11: 55,363,327-55,442,305 , GRCh38.p12 chr11: 55,595,851-55,674,829	OR4C11, OR4C6, 3 more genes
nsv4383892	copy number variation	82	nstd173	human		GRCh37 chr4: 69,435,901-69,485,839 , GRCh38.p12 chr4: 68,570,183-68,620,121	LOC100132651, LOC100422402, 1 more genes
nsv4374696	copy number variation	1	nstd173	human		GRCh37 chr11: 5,783,910-5,812,365 , GRCh38.p12 chr11: 5,762,680-5,791,135	OR52N5, OR52N1, 1 more genes
nsv4382222	copy number variation	125	nstd173	human		GRCh37 chr1: 248,688,587-248,795,289 , GRCh38.p12 chr1: 248,525,286-248,631,988	OR2AS1P, OR2T34, 4 more genes
nsv4386264	copy number variation	1	nstd173	human		GRCh37 chr6: 31,952,483-32,028,339 , GRCh38.p12 chr6: 31,984,706-32,060,562	C4A, C4B, 5 more genes
nsv4386966	copy number variation	2	nstd173	human		GRCh37 chr10: 55,380,381-55,463,941 , GRCh38.p12 chr10: 53,620,621-53,704,181	0
nsv4372727	copy number variation	1	nstd173	human		GRCh37 chr3: 109,918,190-109,943,651 , GRCh38.p12 chr3: 110,199,343-110,224,804	0
nsv4387883	copy number variation	1	nstd173	human		GRCh37 chr5: 45,192,276-45,213,519 , GRCh38.p12 chr5: 45,192,174-45,213,417	0

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

1-1049-003 AND nstd173 (19)
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)