dbVar for Gene (Select 116150) - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv5890529	copy number variation	1	nstd209	human		GRCh38 chr6: 117,705,082-117,705,151 , GRCh37.p13 chr6: 118,026,245-118,026,314	NUS1
nsv5462477	copy number variation	1	nstd206	human		GRCh38 chr6: 117,709,121-117,709,250 , GRCh37.p13 chr6: 118,030,284-118,030,413	NUS1
nsv5381446	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 118,028,088-118,028,178 , GRCh38.p12 chr6: 117,706,925-117,707,015	NUS1
nsv5038830	inversion	1	nstd200	human		GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814	, LOC105377981, 623 more genes
nsv4768325	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 116,734,559-123,648,104 , GRCh38.p12 chr6: 116,413,396-123,326,959	GJA1, RNU4-76P, 80 more genes
nsv4744250	copy number variation	1	nstd199	human		GRCh37 chr6: 117,999,876-118,003,030 , GRCh38.p12 chr6: 117,678,713-117,681,867	NUS1
nsv4599773	copy number variation	1	nstd183	human		GRCh37 chr6: 117,996,417-117,996,486 , GRCh38.p12 chr6: 117,675,254-117,675,323	NUS1, LOC101927919
nsv4457007	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 110,981,075-119,608,396 , GRCh38.p12 chr6: 110,659,872-119,287,231	HDAC2-AS2, NIP7P3, 134 more genes
nsv4456358	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 117,746,455-118,649,226 , GRCh38.p12 chr6: 117,425,292-118,328,063	ROS1, LOC105377967, 10 more genes
nsv4330897	inversion	1	nstd166	human		GRCh37.p13 chr6: 90,629,263-160,387,383 , GRCh38.p12 chr6: 89,919,544-159,966,351	, ACAT2, 894 more genes
nsv4133468	copy number variation	1	nstd166	human		GRCh37.p13 chr6: 118,030,284-118,030,413 , GRCh38.p12 chr6: 117,709,121-117,709,250	NUS1
nsv3924741	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 106,951,594-126,102,365 , GRCh38 chr6: 106,503,719-125,781,219 , NCBI36 chr6: 107,058,287-126,144,058	LOC105377979, LOC105377936, 266 more genes
nsv3924661	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 115,601,230-128,514,324 , GRCh37 chr6: 115,922,394-128,835,469 , NCBI36 chr6: 116,029,087-128,877,162	MCM9, YWHAZP4, 146 more genes
nsv3924576	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 97,164,591-122,524,393 , GRCh38 chr6: 96,609,994-122,161,548 , GRCh37 chr6: 97,057,870-122,482,694	TUBE1, PLN, 318 more genes
nsv3924512	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 118,035,003-127,062,818 , GRCh37 chr6: 117,928,310-127,021,125 , GRCh38 chr6: 117,607,147-126,699,980	HSF2, LOC285762, 85 more genes
nsv3920974	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 118,027,339-118,718,476 , GRCh38 chr6: 117,706,176-118,397,313 , NCBI36 chr6: 118,134,032-118,825,169	SLC35F1, NUS1, 3 more genes
nsv3920683	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 109,372,795-132,430,553 , GRCh37 chr6: 109,266,102-132,388,860 , GRCh38 chr6: 108,944,899-132,067,720	SSXP10, TRE-CTC1-7, 298 more genes
nsv3919913	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr6: 117,634,847-118,309,698 , GRCh37 chr6: 117,528,154-118,203,005 , GRCh38 chr6: 117,206,991-117,881,842	RAP1BP3, DCBLD1, 10 more genes
nsv3919111	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 74,382,807-142,040,500 , NCBI36 chr6: 75,149,243-142,403,330 , GRCh37 chr6: 75,092,523-142,361,637	RNU6-770P, MAP3K5-AS2, 810 more genes
nsv3919038	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr6: 117,243,055-120,081,740 , GRCh37 chr6: 117,136,362-120,040,041 , GRCh38 chr6: 116,815,199-119,718,887	MAN1A1, PLN, 37 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 164

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 164

Page of 9

Number of Variants: 20

Page of 9

Supplemental Content

Find related data

Recent activity