or5au1[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
nsv6314715	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 21,162,263-50,713,602 , GRCh38.p12 chr14: 20,694,104-50,246,884	OR5AU1, HNRNPC, 616 more genes
nsv3916277	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr14: 19,734,944-44,823,755 , GRCh38 chr14: 20,196,945-45,284,802 , GRCh37 chr14: 20,665,104-45,754,005	OR5AU1, MIR208B, 600 more genes
nsv3917301	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 19,755,249-22,741,281 , GRCh37 chr14: 20,223,408-23,210,490 , NCBI36 chr14: 19,293,248-22,280,330	OR5AU1, RNASE8, 271 more genes
nsv6637318	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,690,196-23,114,522 , GRCh38.p12 chr14: 20,222,037-22,645,313	OR5AU1, TRAJ21, 239 more genes
nsv4676085	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 21,143,933-23,297,667 , GRCh38.p12 chr14: 20,675,774-22,828,458	OR5AU1, ANG, 209 more genes
nsv4729394	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,511,672-21,915,516 , GRCh38.p12 chr14: 20,043,513-21,447,357	OR5AU1, SETP1, 99 more genes
nsv3914336	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 20,475,357-21,613,255 , GRCh37 chr14: 20,943,516-22,081,409 , NCBI36 chr14: 20,013,356-21,151,249	OR5AU1, TRP-TGG3-2, 80 more genes
nsv7094244	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,915,399-22,005,055 , GRCh38.p12 chr14: 20,447,240-21,536,921	OR5AU1, ARHGEF40, 78 more genes
nsv3911327	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 21,377,022-22,044,608 , NCBI36 chr14: 20,446,862-21,114,448 , GRCh38 chr14: 20,908,863-21,576,473	OR5AU1, RN7SL650P, 41 more genes
nsv4675976	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 21,589,998-21,999,445 , GRCh38.p12 chr14: 21,121,839-21,531,311	OR5AU1, LOC105378175, 19 more genes
nsv3902883	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,000,422-107,289,053 , GRCh38.p12 chr14: 18,223,945-106,880,863	OR5AU1, LOC440181, 1998 more genes
nsv3907460	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,280,733-107,287,663 , GRCh38.p12 chr14: 18,504,256-106,879,456	OR5AU1, BANF1P1, 1996 more genes
nsv3899639	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,327,823-107,287,663 , GRCh38.p12 chr14: 18,551,346-106,879,456	OR5AU1, LOC100289511, 1996 more genes
nsv3903256	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,794,561-107,234,280 , GRCh38.p12 chr14: 19,652,445-106,826,050	OR5AU1, DHRS7, 1946 more genes
nsv3919106	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,511,673-107,285,437 , GRCh38 chr14: 20,043,514-106,877,229 , NCBI36 chr14: 19,581,513-106,356,482	OR5AU1, SRMP2, 1929 more genes
nsv3904265	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,511,673-107,285,437 , GRCh38.p12 chr14: 20,043,514-106,877,229	OR5AU1, CRIP1, 1929 more genes
nsv3917422	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 20,151,149-106,855,263 , NCBI36 chr14: 19,689,148-106,334,523 , GRCh37 chr14: 20,619,308-107,263,478	OR5AU1, MIR656, 1918 more genes
nsv3913204	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,511,672-49,111,245 , GRCh38 chr14: 20,043,513-48,642,042 , NCBI36 chr14: 19,581,512-48,180,995	OR5AU1, SMARCE1P3, 635 more genes
nsv6315513	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,511,672-47,481,203 , GRCh38.p12 chr14: 20,043,513-47,012,000	OR5AU1, CDH24, 623 more genes
nsv4675943	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,511,672-44,829,030 , GRCh38.p12 chr14: 20,043,513-44,359,827	OR5AU1, TRAJ36, 590 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 43

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 43

Page of 3

Number of Variants: 20

Page of 3

Supplemental Content

Find related data

Search details

Recent activity