"nstd102"[study] AND "duchenne"[Clinical Phenotype] AND "muscular"[Cli - 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
nsv5674197	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 31,462,578-31,986,651 , GRCh38.p12 chrX: 31,444,461-31,968,534	DMD
nsv7098031	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 31,462,578-31,950,364 , GRCh38.p12 chrX: 31,444,461-31,932,247	DMD
nsv7098380	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 31,514,885-31,986,651 , GRCh38.p12 chrX: 31,496,768-31,968,534	DMD
nsv5673991	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 31,514,895-31,986,641 , GRCh38.p12 chrX: 31,496,778-31,968,524	DMD
nsv7098267	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 31,525,378-31,986,651 , GRCh38.p12 chrX: 31,507,261-31,968,534	DMD
nsv5673919	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 31,496,203-31,950,364 , GRCh38.p12 chrX: 31,478,086-31,932,247	DMD
nsv3875940	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 31,496,223-31,950,344 , GRCh38 chrX: 31,478,106-31,932,227	DMD
nsv3877892	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 31,514,885-31,893,510 , GRCh38 chrX: 31,496,768-31,875,393	DMD
nsv3874728	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 31,514,905-31,893,490 , GRCh38 chrX: 31,496,788-31,875,373	DMD
nsv7098653	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 32,662,229-33,038,337 , GRCh38.p12 chrX: 32,644,112-33,020,220	DMD
nsv4681237	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 31,613,687-31,986,641 , GRCh38.p12 chrX: 31,595,570-31,968,524	DMD
nsv3875878	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 31,609,584-31,968,514 , GRCh37 chrX: 31,627,701-31,986,631	DMD
nsv4451871	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 31,609,621-31,968,524 , GRCh37 chrX: 31,627,738-31,986,641	DMD
nsv4682567	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 32,235,023-32,591,973 , GRCh38.p12 chrX: 32,216,906-32,573,856	DMD
nsv3872479	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 31,627,653-31,968,534 , GRCh37.p13 chrX: 31,645,770-31,986,651	DMD
nsv4454570	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 31,627,663-31,968,524 , GRCh37 chrX: 31,645,780-31,986,641	DMD
nsv6313424	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 31,462,578-31,792,329 , GRCh38.p12 chrX: 31,444,461-31,774,212	DMD
nsv7098033	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 31,525,378-31,854,956 , GRCh38.p12 chrX: 31,507,261-31,836,839	DMD
nsv6313077	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 32,235,013-32,563,471 , GRCh38.p12 chrX: 32,216,896-32,545,354	DMD
nsv3872015	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 31,609,621-31,932,247 , GRCh37 chrX: 31,627,738-31,950,364	DMD

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 801

Page of 41

Number of Variants: 20

Page of 41

Supplemental Content

Find related data

Search details

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