MS25864 AND nstd71 - dbVar - NCBI

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

Search results

Items: 11

loading data ...

Number of Variants: 11

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv884822	copy number variation	2547	nstd71	human		NCBI36 chr6: 32,560,168-32,593,470 , GRCh37.p13 chr6: 32,452,190-32,485,492 , GRCh38.p12 chr6: 32,484,413-32,517,715	HLA-DRB5
nsv890754	copy number variation	920	nstd71	human		NCBI36 chr8: 39,350,791-39,509,376 , GRCh37.p13 chr8: 39,231,634-39,390,219 , GRCh38.p12 chr8: 39,374,115-39,532,700	ADAM5, ADAM3A
nsv887800	copy number variation	3	nstd71	human		NCBI36 chr7: 17,447,836-17,549,131 , GRCh37.p13 chr7: 17,481,311-17,582,606 , GRCh38.p12 chr7: 17,441,687-17,542,982	LINC02888, LINC02889, 1 more genes
nsv885516	copy number variation	9	nstd71	human		NCBI36 chr6: 32,703,020-32,718,278 , GRCh37.p13 chr6\|NT_167246.1: 4,051,205-4,066,377 , GRCh37.p13 chr6\|NT_167247.1: 3,933,920-3,949,121 , GRCh37.p13 chr6\|NT_167245.1: 3,876,772-3,891,944 , GRCh37.p13 chr6\|NT_167249.1: 4,028,502-4,043,703 , GRCh37.p13 chr6: 32,595,042-32,610,300 , GRCh38.p12 chr6\|NT_167247.2: 3,928,335-3,943,536 , GRCh38.p12 chr6\|NT_167249.2: 4,029,204-4,044,405 , GRCh38.p12 chr6\|NT_167245.2: 3,871,187-3,886,359 , GRCh38.p12 chr6\|NT_167246.2: 4,045,585-4,060,757 , GRCh38.p12 chr6: 32,627,265-32,642,523	HLA-DQA1, , 2 more genes
nsv883932	copy number variation	140	nstd71	human		NCBI36 chr6: 29,989,443-30,004,400 , GRCh37.p13 chr6: 29,881,464-29,896,421 , GRCh37.p13 chr6\|NT_167246.1: 1,175,640-1,190,626 , GRCh38.p12 chr6: 29,913,687-29,928,644 , GRCh38.p12 chr6\|NT_167246.2: 1,170,020-1,185,006	HLA-K, HCG4B, 1 more genes
nsv883761	copy number variation	45	nstd71	human		NCBI36 chr6: 29,973,697-29,988,619 , GRCh37.p13 chr6\|NT_167246.1: 1,159,894-1,174,816 , GRCh37.p13 chr6: 29,865,718-29,880,640 , GRCh38.p12 chr6: 29,897,941-29,912,863 , GRCh38.p12 chr6\|NT_167246.2: 1,154,274-1,169,196	HLA-A, DDX39BP1, 3 more genes
nsv883570	copy number variation	167	nstd71	human		NCBI36 chr6: 29,957,666-29,972,182 , GRCh37.p13 chr6: 29,849,687-29,864,203 , GRCh38.p12 chr6: 29,881,910-29,896,426	HLA-T, HCG4P7, 1 more genes
nsv908392	copy number variation	32	nstd71	human		NCBI36 chr17: 41,775,690-42,143,493 , GRCh37.p13 chr17: 44,419,932-44,788,310 , GRCh38.p12 chr17: 46,342,566-46,710,944	LRRC37A2, ARL17B, 6 more genes
nsv901263	copy number variation	14	nstd71	human		NCBI36 chr14: 19,249,891-19,494,891 , GRCh37.p13 chr14: 20,180,051-20,425,051 , GRCh38.p12 chr14: 19,711,892-19,956,892	OR4K5, OR4K2, 13 more genes
nsv914608	copy number variation	13	nstd71	human		NCBI36 chr22: 22,600,777-22,728,586 , GRCh37.p13 chr22: 24,270,777-24,398,586 , GRCh38.p12 chr22\|NT_187633.1: 192,395-292,761	MTND1P13, GSTTP2, 10 more genes
nsv884758	copy number variation	27	nstd71	human		NCBI36 chr6: 32,549,254-32,563,460 , GRCh37.p13 chr6: 32,441,276-32,455,482 , GRCh38.p12 chr6: 32,473,499-32,487,705	0

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

MS25864 AND nstd71 (12)
dbVar
MS21314 AND nstd71 (10)
dbVar
MS16808 AND nstd71 (10)
dbVar
MS18377 AND nstd71 (9)
dbVar
Protein Links for Gene (Select 2540614) (2)
Protein

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)