bet1[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
nsv3893823	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 93,602,701-93,668,153 , GRCh38.p12 chr7: 93,973,389-94,038,841	BET1, BET1-AS1
nsv4729398	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 93,588,920-93,783,393 , GRCh38.p12 chr7: 93,959,608-94,154,081	BET1, BET1-AS1
nsv6636693	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 93,539,781-93,623,201 , GRCh38.p12 chr7: 93,910,469-93,993,889	BET1, GNG11, 3 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	BET1, RNU6-438P, 2682 more genes
nsv3888815	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 12,258,147-140,494,267 , GRCh38.p12 chr7: 12,218,521-140,794,467	BET1, LOC107986817, 2014 more genes
nsv3914094	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 84,002,634-95,228,883 , GRCh37 chr7: 83,631,950-94,858,195 , NCBI36 chr7: 83,469,886-94,696,131	BET1, LINC03017, 121 more genes
nsv3892887	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 92,445,452-99,686,985 , GRCh38.p12 chr7: 92,816,138-100,089,362	BET1, LOC105375402, 153 more genes
nsv6636271	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 92,721,627-98,311,537 , GRCh38.p12 chr7: 93,092,314-98,682,225	BET1, MARK2P10, 97 more genes
nsv3911538	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 92,226,394-97,035,894 , GRCh38 chr7: 92,759,144-97,568,646 , GRCh37 chr7: 92,388,458-97,197,958	BET1, LOC105375410, 75 more genes
nsv3908984	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 93,285,237-96,280,817 , GRCh38.p12 chr7: 93,655,925-96,651,505	BET1, LOC105375402, 51 more genes
nsv4685981	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 93,516,132-95,668,733 , GRCh38.p12 chr7: 93,886,820-96,039,421	BET1, LOC105375404, 36 more genes
nsv3916221	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 92,754,488-94,797,369 , GRCh37.p13 chr7: 92,916,552-94,959,433 , GRCh38.p12 chr7: 93,287,240-95,330,121	BET1, BET1-AS1, 33 more genes
nsv3894780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842	BET1, RNU6-565P, 2684 more genes
nsv4455091	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017	BET1, RPL23AP51, 2684 more genes
nsv3909087	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 44,935-159,126,310 , GRCh38.p12 chr7: 44,935-159,333,620	BET1, MNX1-AS2, 2682 more genes
nsv3908592	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr7: 43,361-159,119,707 , GRCh38.p12 chr7: 43,361-159,327,017	BET1, TRGV3, 2682 more genes
nsv5381780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 87,477,185-100,333,327 , GRCh38.p12 chr7: 87,847,870-100,735,704	BET1, ARPC1A, 265 more genes
nsv6315223	complex substitution	1	nstd102	human	Pathogenic	GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017	BET1, AOC1, 2682 more genes
nsv4352523	inversion	1	nstd102	human	Pathogenic	GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550	BET1, ACHE, 1532 more genes
nsv3912266	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr7: 92,412,396-93,979,346 , GRCh37 chr7: 92,574,460-94,141,410 , GRCh38 chr7: 92,945,146-94,512,098	BET1, CALCR, 24 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 25

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 25

Page of 2

Number of Variants: 20

Page of 2

Supplemental Content

Find related data

Search details

Recent activity