vangl1[All Fields] AND 1[has_clinical] - dbVar - NCBI

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

Search results

Items: 19

loading data ...

Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3885225	copy number variation	1	nstd102	human	Benign	GRCh37 chr1: 116,226,658-116,232,765 , GRCh38.p12 chr1: 115,684,037-115,690,144	VANGL1
nsv3886523	copy number variation	1	nstd102	human	Benign	GRCh37 chr1: 116,227,664-116,232,765 , GRCh38.p12 chr1: 115,685,043-115,690,144	VANGL1
nsv3887166	copy number variation	1	nstd102	human	Benign	GRCh37 chr1: 116,230,000-116,234,313 , GRCh38.p12 chr1: 115,687,379-115,691,692	VANGL1
nsv3876156	copy number variation	1	nstd102	human	Benign	GRCh37 chr1: 116,228,152-116,231,289 , GRCh38.p12 chr1: 115,685,531-115,688,668	VANGL1
nsv3881246	copy number variation	1	nstd102	human	Benign	GRCh37 chr1: 116,229,678-116,232,765 , GRCh38.p12 chr1: 115,687,057-115,690,144	VANGL1
nsv3878195	copy number variation	1	nstd102	human	Benign	GRCh37 chr1: 116,232,678-116,296,777 , GRCh38.p12 chr1: 115,690,057-115,754,156	VANGL1, CASQ2
nsv3882130	copy number variation	1	nstd102	human	Benign	GRCh37 chr1: 116,234,313-116,295,007 , GRCh38.p12 chr1: 115,691,692-115,752,386	VANGL1, CASQ2
nsv5381058	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 102,021,465-119,737,478 , GRCh38.p12 chr1: 101,555,909-119,194,855	VANGL1, AMYP1, 320 more genes
nsv3877365	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250	VANGL1, MARK1, 4930 more genes
nsv3885206	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793	VANGL1, SNAP47, 4927 more genes
nsv3884414	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485	VANGL1, RNU1-153P, 4887 more genes
nsv3882464	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 93,837,992-121,343,783 , GRCh38.p12 chr1: 93,372,435-121,601,985	VANGL1, LINC02607, 513 more genes
nsv3890331	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 104,669,629-120,321,801 , GRCh37 chr1: 104,868,106-120,471,049 , GRCh38 chr1: 104,325,484-119,977,655	VANGL1, OR11I1P, 324 more genes
nsv6313671	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 111,647,582-121,343,783 , GRCh38.p12 chr1: 111,104,960-121,601,985	VANGL1, GAPDHP23, 243 more genes
nsv3898188	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 110,100,775-118,994,350 , GRCh38 chr1: 109,756,630-118,650,204 , GRCh37 chr1: 110,299,252-119,192,827	VANGL1, AP4B1-AS1, 198 more genes
nsv4673999	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr1: 114,024,461-116,189,135 , GRCh38.p12 chr1: 113,481,839-115,646,514	VANGL1, AMPD1, 43 more genes
nsv4451097	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 116,105,961-116,397,171 , GRCh38.p12 chr1: 115,563,340-115,854,550	VANGL1, CASQ2, 4 more genes
nsv7095740	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 113,456,513-116,311,162 , GRCh38.p12 chr1: 112,913,891-115,768,541	VANGL1, TRIM33, 55 more genes
nsv3873640	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 116,065,879-116,693,221 , GRCh38.p12 chr1: 115,523,258-116,150,600	VANGL1, CNOT7P2, 12 more genes

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

vangl1[All Fields] AND 1[has_clinical] (20)
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)