asb7[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
nsv4675638	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 101,163,927-101,382,716 , GRCh38.p12 chr15: 100,623,722-100,842,511	ASB7, LOC105371024, 2 more genes
nsv3916249	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189	ASB7, H3P40, 1616 more genes
nsv3919468	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189	ASB7, RNU6-18P, 1442 more genes
nsv4729092	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 86,962,053-102,531,392 , GRCh38.p12 chr15: 86,418,822-101,981,189	ASB7, CHD2, 272 more genes
nsv4675149	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 87,189,245-102,429,112 , GRCh38.p12 chr15: 86,646,014-101,888,909	ASB7, TTLL13, 264 more genes
nsv3908429	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 90,346,994-102,354,798 , GRCh38.p12 chr15: 89,803,763-101,814,595	ASB7, RPL31P55, 201 more genes
nsv3899918	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 92,197,136-102,354,857 , GRCh38.p12 chr15: 91,653,906-101,814,654	ASB7, SNRPCP18, 148 more genes
nsv6112780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 92,335,751-102,399,741 , GRCh38.p12 chr15: 91,792,521-101,859,538	ASB7, LOC105371009, 149 more genes
nsv3919064	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 91,542,950-100,200,996 , GRCh38 chr15: 93,198,717-101,843,270 , GRCh37 chr15: 93,741,946-102,383,473	ASB7, LOC105371032, 126 more genes
nsv3918825	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 94,348,261-101,867,081 , GRCh38 chr15: 93,805,032-101,326,876 , NCBI36 chr15: 92,149,265-99,684,604	ASB7, LOC440311, 107 more genes
nsv3922914	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 92,814,458-100,338,915 , GRCh37.p13 chr15: 95,013,454-102,521,392 , GRCh38.p12 chr15: 94,470,225-101,981,189	ASB7, OR4F14P, 124 more genes
nsv3897684	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 95,136,822-102,045,577 , GRCh38.p12 chr15: 94,593,593-101,505,374	ASB7, ARRDC4, 98 more genes
nsv6313944	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 94,836,128-101,302,111 , GRCh38.p12 chr15: 94,292,899-100,761,906	ASB7, LINC01582, 85 more genes
nsv3921313	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 96,313,856-102,351,195 , NCBI36 chr15: 94,114,860-100,168,718 , GRCh38 chr15: 95,770,627-101,810,992	ASB7, SELENOS, 97 more genes
nsv3923265	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 96,567,356-102,461,201 , NCBI36 chr15: 94,368,360-100,278,724 , GRCh38 chr15: 96,024,127-101,920,998	ASB7, LOC107987228, 104 more genes
nsv3911877	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 94,413,658-100,207,304 , GRCh38 chr15: 96,069,425-101,849,578 , GRCh37 chr15: 96,612,654-102,389,781	ASB7, LOC400464, 99 more genes
nsv4578637	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 96,878,099-102,397,836 , GRCh38.p12 chr15: 96,334,870-101,857,633	ASB7, SYNM-AS1, 94 more genes
nsv3918683	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr15: 96,329,791-101,849,578 , NCBI36 chr15: 94,674,024-100,207,304 , GRCh37 chr15: 96,873,020-102,389,781	ASB7, LYSMD4, 95 more genes
nsv4350607	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 96,873,212-102,389,423 , GRCh38.p12 chr15: 96,329,983-101,849,220	ASB7, LOC105371010, 95 more genes
nsv3891450	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 96,913,435-102,429,112 , GRCh38.p12 chr15: 96,370,206-101,888,909	ASB7, LOC107984790, 96 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 111

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 111

Page of 6

Number of Variants: 20

Page of 6

Supplemental Content

Find related data

Search details

Recent activity