MS18256 AND nstd71 - dbVar - NCBI

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

Search results

Items: 8

loading data ...

Number of Variants: 8

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
nsv893222	copy number variation	50	nstd71	human		NCBI36 chr9: 43,570,503-43,641,682 , GRCh37.p13 chr9: 43,630,507-43,701,686 , GRCh38.p12 chr9: 42,112,703-42,183,882	SPATA31A6, CNTNAP3B
nsv892178	copy number variation	3	nstd71	human		NCBI36 chr9: 6,663,957-6,740,556 , GRCh37.p13 chr9: 6,673,957-6,750,556 , GRCh38.p12 chr9: 6,673,957-6,750,556	LINC02851, RPL35AP20, 3 more genes
nsv913679	copy number variation	1	nstd71	human		NCBI36 chr21: 31,740,623-31,887,245 , GRCh37.p13 chr21: 32,818,752-32,965,374 , GRCh38.p12 chr21: 31,446,439-31,593,061	MTRES1P2, TIAM1, 2 more genes
nsv874647	copy number variation	11	nstd71	human		NCBI36 chr2: 89,731,562-89,911,010 , GRCh37.p13 chr2: 90,094,257-90,273,705 , GRCh38.p12 chr2: 90,055,411-90,234,838	IGKV1D-13, IGKV1D-43, 12 more genes
nsv902515	copy number variation	9	nstd71	human		NCBI36 chr14: 105,083,528-105,217,427 , GRCh37.p13 chr14: 106,012,483-106,146,382 , GRCh37.p13 chr14\|NW_004166863.1: 209,313-343,212 , GRCh38.p12 chr14: 105,546,146-105,680,045 , GRCh38.p12 chr14\|NT_187600.1: 13,144-147,814	LOC107987414, IGHE, 13 more genes
nsv876893	copy number variation	298	nstd71	human		NCBI36 chr3: 65,159,939-65,190,844 , GRCh37.p13 chr3: 65,184,899-65,215,804 , GRCh38.p12 chr3: 65,199,224-65,230,129	0
nsv901920	copy number variation	5	nstd71	human		NCBI36 chr14: 47,535,588-47,549,498 , GRCh37.p13 chr14: 48,465,838-48,479,748 , GRCh38.p12 chr14: 47,996,635-48,010,545	0

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

MS18256 AND nstd71 (9)
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)