lmod2[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
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	LMOD2, 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	LMOD2, LOC107986817, 2014 more genes
nsv3916726	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 116,754,095-134,125,980 , GRCh38 chr7: 117,326,805-134,790,689 , GRCh37 chr7: 116,966,859-134,475,440	LMOD2, LOC107986845, 245 more genes
nsv3900620	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 111,613,396-127,897,316 , GRCh38.p12 chr7: 111,973,341-128,257,263	LMOD2, LSM8, 170 more genes
nsv3916529	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 113,782,532-125,480,435 , NCBI36 chr7: 113,569,768-125,267,671 , GRCh38 chr7: 114,142,477-125,840,381	LMOD2, CAPZA2, 124 more genes
nsv3922792	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 113,227,126-124,326,508 , GRCh37 chr7: 113,439,890-124,539,272 , GRCh38 chr7: 113,799,835-124,899,218	LMOD2, MTND4P6, 116 more genes
nsv5381759	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 116,297,277-126,370,694 , GRCh38.p12 chr7: 116,657,223-126,730,640	LMOD2, TMEM229A, 110 more genes
nsv4455826	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 121,480,906-129,389,003 , GRCh38.p12 chr7: 121,840,852-129,749,163	LMOD2, ASB15, 127 more genes
nsv3923164	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 121,658,176-128,547,780 , GRCh38 chr7: 122,018,122-128,907,727 , NCBI36 chr7: 121,445,412-128,335,016	LMOD2, GCC1, 104 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	LMOD2, 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	LMOD2, 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	LMOD2, 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	LMOD2, TRGV3, 2682 more genes
nsv3922815	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 96,887,100-158,409,214 , GRCh38 chr7: 97,419,852-158,923,762 , GRCh37 chr7: 97,049,164-158,716,453	LMOD2, SEPTIN7P6, 1175 more genes
nsv3894097	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 98,693,388-159,119,707 , GRCh38.p12 chr7: 99,095,765-159,327,017	LMOD2, CYP3A5, 1144 more genes
nsv4675620	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 109,251,060-159,119,707 , GRCh38.p12 chr7: 109,611,003-159,327,017	LMOD2, RPL26P23, 887 more genes
nsv3918979	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 115,099,069-159,118,507 , NCBI36 chr7: 114,886,305-158,811,268 , GRCh38 chr7: 115,459,015-159,325,817	LMOD2, ABCF2, 844 more genes
nsv3917337	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 121,863,759-159,335,865 , NCBI36 chr7: 121,291,049-158,821,316 , GRCh37 chr7: 121,503,813-159,128,555	LMOD2, INSIG1-DT, 776 more genes
nsv6313851	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 106,984,287-128,949,489 , GRCh38.p12 chr7: 107,343,842-129,309,648	LMOD2, DOCK4-AS1, 262 more genes
nsv6315223	complex substitution	1	nstd102	human	Pathogenic	GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017	LMOD2, AOC1, 2682 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 29

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 29

Page of 2

Number of Variants: 20

Page of 2

Supplemental Content

Find related data

Search details

Recent activity