actb[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
nsv4768306	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr7: 5,567,327-5,567,689 , GRCh38 chr7: 5,527,696-5,528,058	ACTB
nsv3906702	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 5,569,364-5,570,221 , GRCh38.p12 chr7: 5,529,733-5,530,590	ACTB
nsv6312451	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 5,567,379-5,569,288 , GRCh38.p12 chr7: 5,527,748-5,529,657	ACTB
nsv7097633	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 5,567,379-5,569,051 , GRCh38.p12 chr7: 5,527,748-5,529,420	ACTB
nsv7097380	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 5,567,615-5,569,051 , GRCh38.p12 chr7: 5,527,984-5,529,420	ACTB
nsv7098125	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 5,567,379-5,568,370 , GRCh38.p12 chr7: 5,527,748-5,528,739	ACTB
nsv6636106	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr7: 5,527,882-5,527,883 , GRCh37 chr7: 5,567,513-5,567,514	ACTB
nsv3916066	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 5,503,372-5,537,444 , GRCh37 chr7: 5,536,846-5,570,918 , GRCh38 chr7: 5,497,215-5,531,287	ACTB, LOC221946, 1 more genes
nsv3910630	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331	DAZAP2P1, RPL36AP16, 2991 more genes
nsv3919826	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840	ACTB, RNU6-438P, 2682 more genes
nsv6290867	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 122,699,106-143,799,629 , GRCh38.p12 chr2: 121,941,530-143,042,060	RNU6-675P, RNU6-1049P, 300 more genes
nsv3876229	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 120,571,363-141,627,287 , GRCh38.p12 chr2: 119,813,787-140,869,718	MIR9986, KLF2P4, 320 more genes
nsv3897428	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 123,445,762-140,592,538 , NCBI36 chr2: 123,919,808-141,066,577 , GRCh37 chr2: 124,203,338-141,350,107	ARHGAP42P2, LOC647996, 278 more genes
nsv3894414	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 118,843,900-135,722,308 , GRCh38 chr2: 118,086,324-134,964,738 , NCBI36 chr2: 118,560,370-135,438,778	RHOQP2, POTEE, 287 more genes
nsv3920006	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 45,130-5,920,006 , GRCh38 chr7: 45,130-5,880,375 , NCBI36 chr7: 140,213-5,886,532	ACTB, RNU6-215P, 120 more genes
nsv3912217	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 5,062,000-6,692,258 , GRCh37 chr7: 5,101,631-6,731,889 , NCBI36 chr7: 5,068,157-6,698,414	ACTB, RBAK-RBAKDN, 45 more genes
nsv6637083	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 4,655,928-5,990,874 , GRCh38.p12 chr7: 4,616,297-5,951,243	ACTB, RN7SL556P, 34 more genes
nsv3924886	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 5,101,631-5,864,814 , GRCh38 chr7: 5,062,000-5,825,183 , NCBI36 chr7: 5,068,157-5,831,340	ACTB, LINC02983, 18 more genes
nsv3919366	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 5,157,150-5,920,006 , GRCh38 chr7: 5,117,519-5,880,375 , NCBI36 chr7: 5,123,676-5,886,532	ACTB, FBXL18, 17 more genes
nsv3911484	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 5,331,115-6,031,221 , GRCh37 chr7: 5,370,746-6,070,852 , NCBI36 chr7: 5,337,272-6,037,378	ACTB, RN7SL556P, 19 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 91

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 91

Page of 5

Number of Variants: 20

Page of 5

Supplemental Content

Find related data

Search details

Recent activity