wdr26[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
nsv4728731	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 224,442,473-224,794,913 , GRCh38.p12 chr1: 224,254,771-224,607,211	WDR26, NVL, 7 more genes
nsv7148187	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 224,304,638-224,434,886 , GRCh37.p13 chr1: 224,492,340-224,622,588	WDR26, NVL, 4 more genes
nsv4674115	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 223,653,722-234,591,807 , GRCh38.p12 chr1: 223,480,380-234,456,061	WDR26, LOC105373163, 258 more genes
nsv4674157	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 222,641,389-228,137,574 , GRCh38.p12 chr1: 222,468,047-227,949,873	WDR26, SRP9, 123 more genes
nsv3908695	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 221,587,658-226,810,656 , GRCh38 chr1: 223,347,693-228,556,332 , GRCh37 chr1: 223,521,035-228,744,033	WDR26, SNAP47, 137 more genes
nsv4728176	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 222,605,125-224,696,628 , GRCh38.p12 chr1: 222,431,783-224,508,926	WDR26, SEPTIN7P13, 52 more genes
nsv5200338	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 223,552,998-224,761,890 , GRCh38.p12 chr1: 223,379,656-224,574,188	WDR26, LOC105373025, 32 more genes
nsv4346523	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 224,340,881-225,147,932 , GRCh38.p12 chr1: 224,153,179-224,960,230	WDR26, RNU6-1008P, 18 more genes
nsv6315349	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 224,432,682-225,142,704 , GRCh38.p12 chr1: 224,244,980-224,955,002	WDR26, DNAJB6P6, 13 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	WDR26, 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	WDR26, 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	WDR26, 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	WDR26, 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	WDR26, 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	WDR26, 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	WDR26, 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	WDR26, 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	WDR26, 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	WDR26, 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	WDR26, HLX-AS1, 740 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 43

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 43

Page of 3

Number of Variants: 20

Page of 3

Supplemental Content

Find related data

Search details

Recent activity