ddx1[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
nsv4453270	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 15,133,366-15,730,846 , GRCh38.p12 chr2: 14,993,242-15,590,722	DDX1, NBAS, 2 more genes
nsv3922331	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr2: 15,258,861-15,902,510 , GRCh37.p13 chr2: 15,341,410-15,985,059 , GRCh38.p12 chr2: 15,201,286-15,844,935	DDX1, NBAS, 3 more genes
nsv4454656	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 15,636,487-15,786,810 , GRCh38.p12 chr2: 15,496,363-15,646,686	DDX1, NBAS, 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	DDX1, CYP1B1-AS1, 1649 more genes
nsv3908896	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 6,671,304-16,243,921 , GRCh38 chr2: 6,531,172-16,103,799 , NCBI36 chr2: 6,588,755-16,161,372	DDX1, RNU6-1288P, 138 more genes
nsv4451022	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 15,631,145-21,729,493 , GRCh38.p12 chr2: 15,491,021-21,506,621	DDX1, RAD51AP2, 82 more genes
nsv6112733	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 15,640,273-19,609,496 , GRCh38.p12 chr2: 15,500,149-19,409,735	DDX1, LOC112267888, 40 more genes
nsv3900054	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 13,664,310-16,228,425 , NCBI36 chr2: 13,721,886-16,273,174 , GRCh37 chr2: 13,804,435-16,409,693	DDX1, RN7SL104P, 16 more genes
nsv6311225	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 15,760,332-17,692,222 , GRCh38.p12 chr2: 15,620,208-17,510,955	DDX1, MYCNUT, 18 more genes
nsv6315390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305	DDX1, 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	DDX1, 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	DDX1, 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	DDX1, 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	DDX1, 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	DDX1, 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	DDX1, 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	DDX1, LOC105373394, 507 more genes
nsv3907033	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 20,341-28,496,035 , GRCh38 chr2: 30,341-28,419,664 , GRCh37 chr2: 30,341-28,642,531	DDX1, GTF3C2-AS1, 434 more genes
nsv3893260	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 17,019-26,541,714 , GRCh38 chr2: 17,019-26,318,846 , NCBI36 chr2: 7,019-26,395,218	DDX1, LOC102723389, 362 more genes
nsv3896997	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 12,770-25,039,694 , GRCh37 chr2: 12,770-25,262,563 , NCBI36 chr2: 2,770-25,116,067	DDX1, LOC105373359, 333 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 32

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 32

Page of 2

Number of Variants: 20

Page of 2

Supplemental Content

Find related data

Search details

Recent activity