msh5[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 12

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Number of Variants: 12

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3877040	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698	MSH5, LOC105378061, 2914 more genes
nsv3879811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083	MSH5, RNU6-411P, 2910 more genes
nsv3887898	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394	MSH5, SOD1P1, 2905 more genes
nsv3889814	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382	MSH5, ITPR3, 2905 more genes
nsv4350067	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650	MSH5, HLA-DPB2, 1001 more genes
nsv3913920	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028	MSH5, TRR-ACG1-2, 1385 more genes
nsv4675941	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 31,036,397-34,088,832 , GRCh38.p12 chr6: 31,068,620-34,121,055	MSH5, AGER, 217 more genes
nsv7097426	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 30,695,893-36,953,949 , GRCh38.p12 chr6: 30,728,116-36,986,173	MSH5, LEMD2, 321 more genes
nsv3870570	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 28,130,359-32,108,367 , GRCh38.p12 chr6: 28,162,581-32,140,590	MSH5, LOC105375002, 345 more genes
nsv7097325	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 30,695,893-31,937,492 , GRCh38.p12 chr6: 30,728,116-31,969,715	MSH5, HCG21, 117 more genes
nsv3876127	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 31,384,577-31,902,308 , GRCh38.p12 chr6: 31,416,800-31,934,531	MSH5, HCP5, 66 more genes
nsv3921657	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr6: 31,773,217-31,934,913 , GRCh37.p13 chr6\|NT_167245.1: 2,950,808-3,112,520 , GRCh37.p13 chr6\|NT_167247.1: 3,044,917-3,154,498 , GRCh37.p13 chr6\|NT_167249.1: 3,054,967-3,159,682 , GRCh37.p13 chr6\|NT_167244.1: 3,037,483-3,141,689 , GRCh37.p13 chr6: 31,665,238-31,826,934 , GRCh38.p12 chr6: 31,697,461-31,859,157 , GRCh38.p12 chr6\|NT_167247.2: 3,039,332-3,148,913 , GRCh38.p12 chr6\|NT_167249.2: 3,055,670-3,160,384 , GRCh38.p12 chr6\|NT_167245.2: 2,945,223-3,106,935 , GRCh38.p12 chr6\|NT_167244.2: 3,087,568-3,191,773	MSH5, CLIC1, 24 more genes

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msh5[All Fields] AND 1[has_clinical] (13)
dbVar
Specific Protein Links for Conserved Domains (Select 239524) (4891)
Protein
protein ASPARTIC PROTEASE IN GUARD CELL 1 [Glycine max]
protein ASPARTIC PROTEASE IN GUARD CELL 1 [Glycine max]
gi|356531224|ref|XP_003534178.1|

Protein
Annotated Genomic for Nucleotide (Select 1771661290) (2)
Nucleotide

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