vash2[All Fields] AND 1[has_clinical] - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3870546	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 213,092,201-213,176,992 , GRCh38.p12 chr1: 212,918,859-213,003,650	VASH2, ANGEL2
nsv3884185	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 213,088,559-213,423,221 , GRCh38.p12 chr1: 212,915,217-213,249,878	VASH2, ANGEL2, 1 more genes
nsv3882823	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 213,123,908-213,423,221 , GRCh38.p12 chr1: 212,950,566-213,249,878	VASH2, RPS6KC1, 1 more genes
nsv3871760	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 213,123,908-213,423,221 , GRCh38 chr1: 212,950,566-213,249,878	VASH2, RPS6KC1, 1 more genes
nsv3882404	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 213,054,159-213,549,122 , GRCh38.p12 chr1: 212,880,817-213,375,779	VASH2, ANGEL2, 2 more genes
nsv4683155	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 213,031,795-213,170,660 , GRCh38.p12 chr1: 212,858,453-212,997,318	VASH2, FLVCR1-DT, 2 more genes
nsv4682831	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 212,955,714-213,125,160 , GRCh38.p12 chr1: 212,782,372-212,951,818	VASH2, NSL1, 6 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	VASH2, 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	VASH2, 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	VASH2, RNU1-153P, 4887 more genes
nsv4450583	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 182,388,773-249,111,240 , GRCh38.p12 chr1: 182,419,638-248,817,041	VASH2, RGS18, 1186 more genes
nsv3881012	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 195,483,439-249,213,000 , GRCh38.p12 chr1: 195,514,309-248,918,801	VASH2, LOC105372928, 1062 more genes
nsv6634372	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485	VASH2, LOC105373279, 1036 more genes
nsv4674140	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 204,045,948-249,218,992 , GRCh38.p12 chr1: 204,076,820-248,924,793	VASH2, RNA5S8, 893 more genes
nsv3897747	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 207,346,642-248,930,485 , GRCh37 chr1: 207,519,987-249,224,684 , NCBI36 chr1: 205,586,610-247,191,307	VASH2, RPS18P3, 793 more genes
nsv3890682	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 209,819,552-249,225,312 , NCBI36 chr1: 207,886,175-247,191,935 , GRCh38 chr1: 209,646,207-248,931,113	VASH2, HLX, 749 more genes
nsv3892818	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 209,963,625-248,918,469 , GRCh37 chr1: 210,136,970-249,212,668 , NCBI36 chr1: 208,203,593-247,179,291	VASH2, LOC105373046, 740 more genes
nsv4684187	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 210,152,794-249,218,992 , GRCh38.p12 chr1: 209,979,449-248,924,793	VASH2, HLX-AS1, 740 more genes
nsv3895767	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 187,143,981-224,299,417 , NCBI36 chr1: 185,379,736-222,553,742 , GRCh37 chr1: 187,113,113-224,487,119	VASH2, LOC107985458, 590 more genes
nsv3889347	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 185,644,663-221,698,833 , GRCh38.p12 chr1: 185,675,531-221,525,491	VASH2, MIR1231, 543 more genes

dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Send to:

Search results

Items: 1 to 20 of 28

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Search details

Recent activity

dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 28

Page of 2

Number of Variants: 20

Page of 2

Supplemental Content

Find related data

Search details

Recent activity