tmsb10[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 17

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3910630	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331	TMSB10, DAZAP2P1, 2991 more genes
nsv6634330	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419	TMSB10, CYP1B1-AS1, 1649 more genes
nsv3877742	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 74,365,484-89,129,064 , GRCh38.p12 chr2: 74,138,357-88,829,551	TMSB10, RNU6-561P, 253 more genes
nsv3886532	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 74,527,522-89,125,488 , GRCh38.p12 chr2: 74,300,395-88,825,975	TMSB10, RNU6-561P, 249 more genes
nsv4451607	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 77,907,114-87,330,965 , GRCh38.p12 chr2: 77,679,988-87,103,842	TMSB10, REEP1, 134 more genes
nsv6112750	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 81,209,244-86,688,030 , GRCh38.p12 chr2: 80,982,120-86,460,907	TMSB10, VAMP8, 86 more genes
nsv6313890	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 82,486,900-87,322,042 , GRCh38.p12 chr2: 82,259,776-87,094,919	TMSB10, LOC105374836, 93 more genes
nsv6315390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305	TMSB10, LOC112268439, 3737 more genes
nsv3874648	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305	TMSB10, IGKV2OR2-10, 3737 more genes
nsv3885544	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609	TMSB10, RNU6-674P, 3735 more genes
nsv3882615	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232	TMSB10, MTND2P22, 3724 more genes
nsv3916821	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 47,701,031-86,783,356 , GRCh37.p13 chr2: 47,847,527-86,929,845 , GRCh38.p12 chr2: 47,620,388-86,702,722	TMSB10, NAGK, 595 more genes
nsv3883931	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 63,671,346-85,698,002 , GRCh38.p12 chr2: 63,444,212-85,470,879	TMSB10, LINC01888, 367 more genes
nsv3897079	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 77,025,216-90,282,666 , NCBI36 chr2: 77,105,850-90,982,989 , GRCh37 chr2: 77,252,342-91,619,262	TMSB10, IGKV2D-18, 280 more genes
nsv6314726	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196	TMSB10, ACTG2, 1713 more genes
nsv3903805	copy number variation	1	nstd102	human	Benign	GRCh37 chr2: 7,635,254-88,005,418 , NCBI36 chr2: 7,552,705-87,786,533 , GRCh38 chr2: 7,495,123-87,705,899	TMSB10, LOC101927723, 1246 more genes
nsv3882844	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 82,517,612-86,262,705 , GRCh38.p12 chr2: 82,290,488-86,035,582	TMSB10, TMEM150A, 69 more genes

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tmsb10[All Fields] AND 1[has_clinical] (18)
dbVar
B4GALT1 beta-1,4-galactosyltransferase 1 [Homo sapiens]
B4GALT1 beta-1,4-galactosyltransferase 1 [Homo sapiens]
Gene ID:2683

Gene
Gene Links for GEO Profiles (Select 13283710) (1)
Gene
Related DataSets for GEO Profiles (Select 13300799) (1)
GEO DataSets
Essential thrombocythemia
Essential thrombocythemia
Accession: GDS1376

GEO DataSets

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