ltbp1[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
nsv4673910	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 33,318,508-33,508,810 , GRCh38.p12 chr2: 33,093,441-33,283,743	LTBP1, TYW1P1
nsv4674420	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 33,090,481-33,214,793 , GRCh38.p12 chr2: 32,865,414-32,989,726	LTBP1, LINC00486, 1 more genes
nsv6634330	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419	LTBP1, CYP1B1-AS1, 1649 more genes
nsv6313619	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 29,899,368-42,441,440 , GRCh38.p12 chr2: 29,676,502-42,214,300	LTBP1, LOC107985870, 161 more genes
nsv4454991	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 29,940,473-36,813,297 , GRCh38.p12 chr2: 29,717,607-36,586,154	LTBP1, LOC105374435, 71 more genes
nsv4453170	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 31,958,977-33,946,495 , GRCh38.p12 chr2: 31,733,908-33,721,428	LTBP1, ATP6V0E1P3, 30 more genes
nsv1398102	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 32,348,594-33,632,523 , GRCh38.p12 chr2: 32,123,525-33,407,456	LTBP1, TYW1P1, 16 more genes
nsv6315390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305	LTBP1, LOC112268439, 3737 more genes
nsv3874648	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305	LTBP1, IGKV2OR2-10, 3737 more genes
nsv3885544	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609	LTBP1, RNU6-674P, 3735 more genes
nsv3882615	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232	LTBP1, MTND2P22, 3724 more genes
nsv3908605	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 66,097-55,797,773 , GRCh38 chr2: 66,097-55,570,637 , NCBI36 chr2: 56,097-55,651,277	LTBP1, SLC35F6, 801 more genes
nsv3908288	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 236,816-46,210,371 , GRCh38 chr2: 236,816-45,983,232 , NCBI36 chr2: 226,816-46,063,875	LTBP1, ALLC, 674 more genes
nsv6636815	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 706,460-35,523,639 , GRCh38.p12 chr2: 706,460-35,298,573	LTBP1, LOC105374455, 504 more genes
nsv3908038	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 12,770-33,936,576 , NCBI36 chr2: 2,770-33,790,080 , GRCh38 chr2: 12,770-33,711,509	LTBP1, LOC105373394, 507 more genes
nsv3875055	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 27,861,707-60,790,985 , GRCh38.p12 chr2: 27,638,840-60,563,850	LTBP1, RPL7P13, 426 more genes
nsv3879320	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 22,665,048-52,850,368 , GRCh38.p12 chr2: 22,442,176-52,623,230	LTBP1, ATL2, 465 more genes
nsv6137788	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 24,601,818-43,466,284 , GRCh38.p12 chr2: 24,378,949-43,239,145	LTBP1, GTF3C2-AS1, 316 more genes
nsv3877469	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 28,069,882-43,543,420 , GRCh38.p12 chr2: 27,847,015-43,316,281	LTBP1, FOSL2, 219 more genes
nsv3919769	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 22,776,056-33,845,581 , GRCh37.p13 chr2: 22,922,551-33,992,077 , GRCh38.p12 chr2: 22,699,679-33,767,010	LTBP1, RNA5SP88, 213 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 34

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 34

Page of 2

Number of Variants: 20

Page of 2

Supplemental Content

Find related data

Search details

Recent activity