dbVar for Gene (Select 51329) - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv5973346	inversion	1	nstd209	human		GRCh38 chr12: 118,054,601-123,705,841 , GRCh37.p13 chr12: 118,492,406-124,190,388	, ACADS, 162 more genes
nsv5930736	copy number variation	1	nstd209	human		GRCh38 chr12: 122,981,307-122,981,375 , GRCh37.p13 chr12: 123,465,854-123,465,922	ARL6IP4
nsv4993814	copy number variation	1	nstd200	human		GRCh38 chr12: 122,969,891-122,988,773 , GRCh37.p13 chr12: 123,454,438-123,473,320	PITPNM2, ARL6IP4, 2 more genes
nsv4829410	copy number variation	1	nstd200	human		GRCh37 chr12: 123,454,438-123,473,320 , GRCh38.p12 chr12: 122,969,891-122,988,773	ARL6IP4, OGFOD2, 2 more genes
nsv4756208	inversion	1	nstd199	human		GRCh37 chr12: 104,359,633-125,801,147 , GRCh38.p12 chr12: 103,965,855-125,316,601	, ACACB, 453 more genes
nsv4755205	inversion	1	nstd199	human		GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605	, ACACB, 1787 more genes
nsv4754840	inversion	1	nstd199	human		GRCh37 chr12: 104,382,539-125,801,164 , GRCh38.p12 chr12: 103,988,761-125,316,618	, ACACB, 452 more genes
nsv4736781	copy number variation	1	nstd199	human		GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602	, RNA5SP368, 1787 more genes
nsv4455692	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 122,169,403-129,084,163 , GRCh38.p12 chr12: 121,731,497-128,599,618	LOC107987176, LRRC43, 147 more genes
nsv4221273	copy number variation	1	nstd166	human		GRCh37.p13 chr12: 123,460,630-123,463,617 , GRCh38.p12 chr12: 122,976,083-122,979,070	ARL6IP4, OGFOD2
nsv3924220	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr12: 115,131,583-133,166,920 , NCBI36 chr12: 114,053,771-132,253,579 , GRCh37 chr12: 115,569,388-133,743,506	LOC105370080, LINC02985, 376 more genes
nsv3923612	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr12: 120,718,786-127,500,215 , GRCh37 chr12: 121,156,589-127,984,760 , NCBI36 chr12: 119,640,972-126,550,713	NCOR2, LOC105378258, 161 more genes
nsv3923347	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 119,619,858-132,289,149 , GRCh37 chr12: 121,135,475-133,779,076 , GRCh38 chr12: 120,697,672-133,202,490	LOC105370044, RNU6-1017P, 273 more genes
nsv3920557	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 118,603,264-133,758,908 , GRCh38 chr12: 118,165,459-133,182,322 , NCBI36 chr12: 117,087,647-132,268,981	TMED2, GCN1, 339 more genes
nsv3917475	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr12: 121,697,487-122,107,919 , GRCh38 chr12: 122,646,987-123,057,419 , GRCh37 chr12: 123,131,534-123,541,966	CCDC62, HCAR2, 12 more genes
nsv3916210	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 122,355,664-128,287,262 , GRCh38 chr12: 121,917,758-127,802,717 , NCBI36 chr12: 120,840,047-126,853,215	RILPL2, TCTN2, 129 more genes
nsv3914194	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 100,698-132,283,466 , GRCh37 chr12: 282,465-133,773,393 , GRCh38 chr12: 121,271-133,196,807	, BTG1P1, 2451 more genes
nsv3913894	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 113,190,591-132,287,975 , GRCh38 chr12: 114,268,403-133,201,316 , GRCh37 chr12: 114,706,208-133,777,902	TAOK3, LINC02405, 386 more genes
nsv3908979	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 122,938,957-123,747,037 , GRCh38.p12 chr12: 122,454,410-123,262,490	ZCCHC8, MIR4304, 19 more genes
nsv3905447	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316	, LOH12CR2, 2452 more genes

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Number of Variants: 20

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Items: 1 to 20 of 122

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Number of Variants: 20

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