dbVar for Gene (Select 54998) - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7139049	copy number variation	1	nstd232	human		GRCh37.p13 chr1: 1,309,282-1,309,378 , GRCh38.p12 chr1: 1,373,902-1,373,998	AURKAIP1
nsv7137045	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 536,777-6,012,896 , GRCh38.p12 chr1: 601,397-5,952,836	MIR200B, LOC105378608, 172 more genes
nsv7099018	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 1-2,580,976 , GRCh38.p12 chr1: 10,001-2,649,537	DVL1, LOC100129534, 148 more genes
nsv7044270	inversion	1	nstd229	human		GRCh38 chr1: 1,133,718-2,842,494 , GRCh37.p13 chr1: 1,069,098-2,759,059	LOC105378586, MIR6726, 91 more genes
nsv6641511	copy number variation	1	nstd229	human		GRCh38 chr1: 1,369,517-1,378,228 , GRCh37.p13 chr1: 1,304,897-1,313,608	AURKAIP1, NDUFB4P8
nsv6641321	copy number variation	1	nstd229	human		GRCh38 chr1: 1,362,101-1,372,000 , GRCh37.p13 chr1: 1,297,481-1,307,380	AURKAIP1, MXRA8
nsv6641298	copy number variation	1	nstd229	human		GRCh38 chr1: 1,326,035-1,396,309 , GRCh37.p13 chr1: 1,261,415-1,331,689	DVL1, CPTP, 6 more genes
nsv6641088	copy number variation	1	nstd229	human		GRCh38 chr1: 1,368,831-1,377,461 , GRCh37.p13 chr1: 1,304,211-1,312,841	NDUFB4P8, AURKAIP1
nsv6637093	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 849,467-12,448,956 , GRCh38.p12 chr1: 914,087-12,388,897	VWA1, CEP104, 311 more genes
nsv6636661	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 1,130,311-2,397,177 , GRCh38.p12 chr1: 1,194,931-2,465,738	ATAD3C, ACAP3, 69 more genes
nsv6636292	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 849,467-2,972,435 , GRCh38.p12 chr1: 914,087-3,055,871	LOC105378602, LOC105378599, 108 more genes
nsv6625737	copy number variation	1	nstd224	human		GRCh37 chr1: 1,262,366-2,066,702 , GRCh38.p12 chr1: 1,326,986-2,135,263	GNB1, SLC35E2A, 44 more genes
nsv6320143	copy number variation	1	nstd223	human		GRCh38 chr1: 1,362,087-1,372,098 , GRCh37.p13 chr1: 1,297,467-1,307,478	AURKAIP1, MXRA8
nsv6315818	copy number variation	1	nstd223	human		GRCh38 chr1: 1,372,786-1,375,705 , GRCh37.p13 chr1: 1,308,166-1,311,085	AURKAIP1
nsv6315409	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 849,466-10,258,804 , GRCh38.p12 chr1: 914,086-10,198,746	VAMP3, CTNNBIP1, 245 more genes
nsv6315371	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 849,466-2,518,608 , GRCh38.p12 chr1: 914,086-2,587,169	LINC01786, MMP23A, 96 more genes
nsv6315344	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 849,466-4,183,006 , GRCh38.p12 chr1: 914,086-4,122,946	DFFB, LOC105378604, 136 more genes
nsv6315170	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 834,101-7,930,605 , GRCh38.p12 chr1: 898,721-7,870,545	PRDM16-DT, CAMTA1-AS1, 186 more genes
nsv6314841	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 817,861-1,836,133 , GRCh37.p13 chr1: 753,241-1,767,572	LOC105378948, C1QTNF12, 76 more genes
nsv6310988	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 989,123-3,160,711 , GRCh38.p12 chr1: 1,053,743-3,244,147	GNB1-DT, LOC107984909, 104 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:

Links from Gene

Items: 1 to 20 of 632

Number of Variants: 20

Send to:

Supplemental Content

Find related data

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

Links from Gene

Items: 1 to 20 of 632

Page of 32

Number of Variants: 20

Page of 32

Supplemental Content

Find related data

Recent activity