kcnq3[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
nsv5674053	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 133,141,509-133,492,779 , GRCh38.p12 chr8: 132,129,262-132,480,532	KCNQ3
nsv4683489	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr8: 133,192,384-133,198,448 , GRCh38.p12 chr8: 132,180,137-132,186,201	KCNQ3
nsv3909601	copy number variation	1	nstd102	human	Benign	GRCh37 chr8: 133,226,397-133,306,801 , GRCh38.p12 chr8: 132,214,150-132,294,554	KCNQ3
nsv7098160	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 133,141,509-133,175,761 , GRCh38.p12 chr8: 132,129,262-132,163,514	KCNQ3
nsv7093098	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 133,492,703-133,492,753 , GRCh38 chr8: 132,480,456-132,480,506	KCNQ3
nsv6312902	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 133,141,509-133,198,448 , GRCh38.p12 chr8: 132,129,262-132,186,201	KCNQ3
nsv4682666	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 133,141,499-133,198,438 , GRCh38.p12 chr8: 132,129,252-132,186,191	KCNQ3
nsv7097786	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 133,492,374-133,492,779 , GRCh38.p12 chr8: 132,480,127-132,480,532	KCNQ3
nsv3897543	copy number variation	1	nstd102	human	Benign	GRCh37 chr8: 132,822,037-133,262,048 , GRCh38.p12 chr8: 131,809,790-132,249,801	KCNQ3, EFR3A, 3 more genes
nsv6637812	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 132,732,273-133,269,561 , GRCh38.p12 chr8: 131,720,026-132,257,314	KCNQ3, EFR3A, 3 more genes
nsv4456435	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 132,812,544-133,251,797 , GRCh38.p12 chr8: 131,800,297-132,239,550	KCNQ3, EFR3A, 3 more genes
nsv3910787	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr8: 131,770,098-132,203,964 , GRCh37 chr8: 132,782,345-133,216,211 , NCBI36 chr8: 132,851,527-133,285,393	KCNQ3, HHLA1, 3 more genes
nsv3909347	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 132,812,614-133,245,950 , GRCh38.p12 chr8: 131,800,367-132,233,703	KCNQ3, OC90, 3 more genes
nsv6290789	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 133,055,346-133,267,468 , GRCh38.p12 chr8: 132,043,099-132,255,221	KCNQ3, OC90, 1 more genes
nsv6637224	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 112,234,557-133,668,379 , GRCh38.p12 chr8: 111,222,328-132,656,133	KCNQ3, RNU4-37P, 220 more genes
nsv4674996	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 126,892,814-143,750,028 , GRCh38.p12 chr8: 125,880,570-142,668,610	KCNQ3, POU5F1B, 158 more genes
nsv3915490	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 127,707,788-144,459,935 , GRCh37.p13 chr8: 127,638,606-144,388,560 , GRCh38.p12 chr8: 126,626,361-143,306,390	KCNQ3, LOC107986906, 179 more genes
nsv4455511	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 124,120,772-135,265,846 , GRCh38.p12 chr8: 123,108,532-134,253,603	KCNQ3, MTSS1, 148 more genes
nsv3915853	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 129,176,782-134,170,188 , GRCh37 chr8: 130,189,028-135,182,431 , NCBI36 chr8: 130,258,210-135,251,613	KCNQ3, RPL32P20, 52 more genes
nsv5673945	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr8: 133,141,509-134,296,554 , GRCh38.p12 chr8: 132,129,262-133,284,311	KCNQ3, SLA, 15 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 76

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 76

Page of 4

Number of Variants: 20

Page of 4

Supplemental Content

Find related data

Search details

Recent activity