SP54063 AND nstd71 - dbVar - NCBI

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

Search results

Items: 12

loading data ...

Number of Variants: 12

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv876719	copy number variation	2	nstd71	human		NCBI36 chr3: 41,514,644-41,555,968 , GRCh37.p13 chr3: 41,539,640-41,580,964 , GRCh38.p12 chr3: 41,498,149-41,539,473	ULK4
nsv884818	copy number variation	499	nstd71	human		NCBI36 chr6: 32,560,168-32,591,507 , GRCh37.p13 chr6: 32,452,190-32,483,529 , GRCh38.p12 chr6: 32,484,413-32,515,752	HLA-DRB5
nsv889263	copy number variation	249	nstd71	human		NCBI36 chr7: 141,410,335-141,441,259 , GRCh37.p13 chr7\|NW_003571040.1: 206,017-236,941 , GRCh37.p13 chr7: 141,763,866-141,794,790 , GRCh38.p12 chr7: 142,064,066-142,094,990 , GRCh38.p12 chr7\|NT_187562.1: 25,946-56,870	MGAM
nsv909839	copy number variation	966	nstd71	human		NCBI36 chr18: 64,895,268-64,909,808 , GRCh37.p13 chr18: 66,744,288-66,758,828 , GRCh38.p12 chr18: 69,077,051-69,091,591	CCDC102B
nsv881222	copy number variation	185	nstd71	human		NCBI36 chr4: 162,058,162-162,152,452 , GRCh37.p13 chr4: 161,838,712-161,933,002 , GRCh38.p12 chr4: 160,917,560-161,011,850	LOC105377513
nsv890336	copy number variation	2	nstd71	human		NCBI36 chr8: 8,434,086-8,537,972 , GRCh37.p13 chr8: 8,396,676-8,500,562 , GRCh38.p12 chr8: 8,539,166-8,643,052 , GRCh38.p12 chr8\|NW_018654717.1: 4,709,059-4,812,932	RN7SL178P, LOC105379224
nsv911912	copy number variation	43	nstd71	human		NCBI36 chr19: 48,060,801-48,160,500 , GRCh37.p13 chr19: 43,368,961-43,468,660 , GRCh38.p12 chr19: 42,864,809-42,964,508	CEACAMP7, PSG1, 2 more genes
nsv879318	copy number variation	371	nstd71	human		NCBI36 chr4: 69,085,989-69,179,871 , GRCh37.p13 chr4: 69,403,394-69,497,276 , GRCh38.p12 chr4: 68,537,676-68,631,558	LOC728807, UGT2B17, 2 more genes
nsv881742	copy number variation	4	nstd71	human		NCBI36 chr5: 63,715,205-63,807,817 , GRCh37.p13 chr5: 63,679,449-63,772,061 , GRCh38.p12 chr5: 64,383,622-64,476,234	0
nsv887576	copy number variation	7	nstd71	human		NCBI36 chr7: 10,015,056-10,062,801 , GRCh37.p13 chr7: 10,048,531-10,096,276 , GRCh38.p12 chr7: 10,008,904-10,056,649	0
nsv903270	copy number variation	10	nstd71	human		NCBI36 chr15: 19,768,826-19,993,878 , GRCh37.p13 chr15: 22,267,462-22,492,514 , GRCh38.p12 chr15: 21,979,511-22,204,563	OR4Q1P, OR4M2-OT1, 14 more genes
nsv886565	copy number variation	3	nstd71	human		NCBI36 chr6: 117,602,819-117,686,278 , GRCh37.p13 chr6: 117,496,126-117,579,585 , GRCh38.p12 chr6: 117,174,963-117,258,422	0

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

SP54063 AND nstd71 (13)
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)