dbVar for Gene (Select 11023) - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6112765	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 118,247,181-135,435,319 , GRCh38.p12 chr10: 116,487,669-133,621,815	STK32C, LOC105378542, 266 more genes
nsv5974801	inversion	1	nstd209	human		GRCh38 chr10: 116,446,135-119,236,441 , GRCh37.p13 chr10: 118,205,647-120,995,953	EMX2, PRLHR, 48 more genes
nsv5590581	copy number variation	1	nstd207	human		GRCh38 chr10: 117,126,450-117,126,533 , GRCh37.p13 chr10: 118,885,961-118,886,044	VAX1, SHTN1
nsv5500547	copy number variation	1	nstd206	human		GRCh38 chr10: 117,061,313-117,431,413 , GRCh37.p13 chr10: 118,820,824-119,190,924	SLC18A2, VAX1, 7 more genes
nsv4479028	mobile element insertion	1	nstd166	human		GRCh37.p13 chr10: 118,888,004-118,888,004 , GRCh38.p12 chr10: 117,128,493-117,128,493	VAX1
nsv4456626	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 114,544,537-135,427,143 , GRCh38.p12 chr10: 112,784,778-133,613,639	LOC105378521, ZRANB1, 317 more genes
nsv4349508	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 117,024,753-124,942,806 , GRCh38.p12 chr10: 115,265,276-123,183,290	PRLHR, LOC105378513, 121 more genes
nsv4348764	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 110,022,170-135,439,095 , GRCh38.p12 chr10: 108,262,412-133,625,591	LOC105378492, VENTX, 373 more genes
nsv4342336	sequence alteration	1	nstd166	human		GRCh37.p13 chr10: 118,638,442-121,163,255 , GRCh38.p12 chr10: 116,878,931-119,403,743	EIF3A, VAX1, 38 more genes
nsv3923859	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 113,062,847-135,284,168 , GRCh37 chr10: 113,072,857-135,434,178 , GRCh38 chr10: 111,313,099-133,620,674	AS-PTPRE, SFXN4, 330 more genes
nsv3923769	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 100,194,215-132,432,797 , GRCh37 chr10: 101,953,972-134,246,301 , NCBI36 chr10: 101,943,962-134,096,291	LOC105378493, LINC02627, 477 more genes
nsv3922274	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr10: 103,274,160-135,374,737 , GRCh37.p13 chr10: 103,284,170-135,524,747 , GRCh38.p12 chr10: 101,524,413-133,787,422	DPCD, LOC105378467, 504 more genes
nsv3921919	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 100,600,492-133,622,588 , GRCh37 chr10: 102,360,249-135,436,092 , NCBI36 chr10: 102,350,239-135,286,082	MIR4295, BORCS7, 508 more genes
nsv3920295	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 81,675,342-135,374,737 , GRCh37.p13 chr10: 81,685,362-135,524,747 , GRCh38.p12 chr10: 79,925,606-133,787,422	EIF2S2P3, CYP17A1-AS1, 895 more genes
nsv3919820	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 107,191,100-118,761,489 , GRCh37 chr10: 108,950,858-120,521,001 , NCBI36 chr10: 108,940,848-120,510,991	CCDC186, RN7SKP288, 147 more genes
nsv3914619	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 111,418,518-126,431,209 , GRCh37.p13 chr10: 111,428,528-126,441,219 , GRCh38.p12 chr10: 109,668,770-124,752,650	LOC103344931, LINC02626, 225 more genes
nsv3912079	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 109,852,335-135,284,168 , GRCh38 chr10: 108,102,587-133,620,674 , GRCh37 chr10: 109,862,345-135,434,178	TUBGCP2, SHOC2, 372 more genes
nsv3911931	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 118,114,834-135,324,715 , GRCh37.p13 chr10: 118,124,844-135,474,725 , GRCh38.p12 chr10: 116,365,332-133,661,221	LOC105378571, RPL21P16, 274 more genes
nsv3911051	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr10: 114,450,935-122,720,120 , GRCh37 chr10: 114,460,945-122,730,130 , GRCh38 chr10: 112,701,186-120,970,617	ADRB1, CASP7, 123 more genes
nsv3908254	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 106,003,533-135,427,143 , GRCh38.p12 chr10: 104,243,775-133,613,639	MIR4680, BCCIP, 404 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 116

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 116

Page of 6

Number of Variants: 20

Page of 6

Supplemental Content

Find related data

Recent activity