dbVar for Gene (Select 51122) - 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
nsv5381765	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 138,173,683-162,494,699 , GRCh38.p12 chr3: 138,454,841-162,776,911	MBNL1-AS1, LOC107986138, 339 more genes
nsv5367099	translocation	1	nstd200	human		GRCh38 chr22: 23,665,327-23,665,327 , GRCh38 chr3: 149,740,747-149,740,747 , GRCh37.p13 chr22: 24,007,514-24,007,514 , GRCh37.p13 chr3: 149,458,534-149,458,534	COMMD2, GUSBP11
nsv5352030	translocation	1	nstd200	human		GRCh38 chr3: 149,750,681-149,750,681 , GRCh38 chr3: 149,741,720-149,741,720 , GRCh37.p13 chr3: 149,468,468-149,468,468 , GRCh37.p13 chr3: 149,459,507-149,459,507	COMMD2
nsv5033132	inversion	1	nstd200	human		GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130	, LOC105374154, 433 more genes
nsv4912338	copy number variation	1	nstd200	human		GRCh38 chr3: 149,749,995-149,750,110 , GRCh37.p13 chr3: 149,467,782-149,467,897	COMMD2
nsv4797966	copy number variation	1	nstd200	human		GRCh37 chr3: 149,467,782-149,467,897 , GRCh38.p12 chr3: 149,749,995-149,750,110	COMMD2
nsv4797965	copy number variation	1	nstd200	human		GRCh37 chr3: 149,456,736-149,456,900 , GRCh38.p12 chr3: 149,738,949-149,739,113	COMMD2
nsv4713761	copy number variation	1	nstd195	human		GRCh37 chr3: 149,163,601-149,503,101 , GRCh38.p12 chr3: 149,445,814-149,785,314	FKBP1AP4, TM4SF4, 7 more genes
nsv4684209	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 138,145,289-162,275,610 , GRCh38.p12 chr3: 138,426,447-162,557,822	MTAPP1, PLS1, 339 more genes
nsv4674717	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr3: 144,053,029-150,272,658 , GRCh38.p12 chr3: 144,334,187-150,554,871	AGTR1, CP, 83 more genes
nsv4674301	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 149,404,255-152,786,331 , GRCh38.p12 chr3: 149,686,468-153,068,542	EIF3JP2, IGSF10, 63 more genes
nsv4327395	inversion	1	nstd166	human		GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842	, ACTG1P1, 1039 more genes
nsv4327115	inversion	1	nstd166	human		GRCh37.p13 chr3: 131,882,701-162,233,318 , GRCh38.p12 chr3: 132,163,857-162,515,530	, ATP1B3, 446 more genes
nsv4108818	copy number variation	1	nstd166	human		GRCh37.p13 chr3: 149,468,639-149,469,189 , GRCh38.p12 chr3: 149,750,852-149,751,402	COMMD2
nsv3918981	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446	LINC02614, LINC02054, 1469 more genes
nsv3918784	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 147,160,353-178,240,319 , GRCh38 chr3: 147,442,566-178,522,531 , NCBI36 chr3: 148,643,043-179,723,013	LOC105374167, LOC105374187, 394 more genes
nsv3918692	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 147,521,892-198,096,565 , GRCh37 chr3: 147,239,679-197,823,436 , NCBI36 chr3: 148,722,369-199,307,833	LOC105374179, LINC02038, 785 more genes
nsv3889228	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115	NDUFB4, LOC105374108, 2876 more genes
nsv3887637	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 148,425,748-153,220,169 , GRCh38.p12 chr3: 148,707,961-153,502,380	LOC101927942, FKBP1AP4, 97 more genes
nsv3885606	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156	RNU4-62P, SEMA3B-AS1, 2880 more genes

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Number of Variants: 20

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