dbVar for Gene (Select 101927464) - 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
nsv5381782	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 123,878,845-126,829,341 , GRCh38.p12 chr12: 123,394,298-126,344,795	DDX55, ZNF664, 55 more genes
nsv4996287	copy number variation	1	nstd200	human		GRCh38 chr12: 126,099,651-126,107,540 , GRCh37.p13 chr12: 126,584,197-126,592,086	LINC02359
nsv4996286	copy number variation	1	nstd200	human		GRCh38 chr12: 126,092,250-126,095,560 , GRCh37.p13 chr12: 126,576,796-126,580,106	LINC02359
nsv4996282	copy number variation	1	nstd200	human		GRCh38 chr12: 126,066,300-126,503,199 , GRCh37.p13 chr12: 126,550,846-126,987,745	, LINC02350, 9 more genes
nsv4993847	copy number variation	1	nstd200	human		GRCh38 chr12: 126,032,740-126,418,205 , GRCh37.p13 chr12: 126,517,286-126,902,751	, LOC105379613, 7 more genes
nsv4837410	copy number variation	1	nstd200	human		GRCh37 chr12: 126,550,846-126,987,745 , GRCh38.p12 chr12: 126,066,300-126,503,199	, LOC105379613, 9 more genes
nsv4529464	copy number variation	1	nstd166	human		GRCh37.p13 chr12: 126,464,999-126,727,000 , GRCh38.p12 chr12: 125,980,453-126,242,454	, LINC00939, 6 more genes
nsv4502202	mobile element insertion	1	nstd166	human		GRCh37.p13 chr12: 126,582,401-126,582,401 , GRCh38.p12 chr12: 126,097,855-126,097,855	LINC02359
nsv4456888	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 126,470,636-133,777,902 , GRCh38.p12 chr12: 125,986,090-133,201,316	LINC02347, LOC107987176, 145 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
nsv4385263	copy number variation	1	nstd173	human		GRCh37 chr12: 126,463,562-126,727,689 , GRCh38.p12 chr12: 125,979,016-126,243,143	, LINC00939, 6 more genes
nsv4384450	copy number variation	1	nstd173	human		GRCh37 chr12: 126,463,562-126,720,475 , GRCh38.p12 chr12: 125,979,016-126,235,929	, LOC100420118, 6 more genes
nsv4370349	copy number variation	1	nstd173	human		GRCh37 chr12: 126,463,562-126,726,862 , GRCh38.p12 chr12: 125,979,016-126,242,316	, LINC02359, 6 more genes
nsv4349911	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 125,451,405-133,810,935 , GRCh38.p12 chr12: 124,966,859-133,234,349	LOC107987177, GOLGA3, 159 more genes
nsv4340784	sequence alteration	1	nstd166	human		GRCh37.p13 chr12: 126,578,516-126,583,195 , GRCh38.p12 chr12: 126,093,970-126,098,649	LINC02359
nsv4224012	copy number variation	1	nstd166	human		GRCh37.p13 chr12: 126,576,796-126,580,106 , GRCh38.p12 chr12: 126,092,250-126,095,560	LINC02359
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
nsv3921145	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 123,929,305-133,767,986 , GRCh38 chr12: 123,444,758-133,191,400 , NCBI36 chr12: 122,495,258-132,278,059	ZNF268, PTP4A1P2, 193 more genes

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Items: 1 to 20 of 108

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Number of Variants: 20

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