"nstd102"[study] AND "deletion"[variant_type] - 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
nsv4681940	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 64,776,231-65,336,138 , GRCh38.p12 chr6: 64,066,338-64,626,245	EYS
nsv3876238	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 69,899,499-70,435,751 , GRCh37.p13 chr7: 69,364,485-69,900,737	AUTS2
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
nsv6634656	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 31,525,571-31,947,712 , GRCh38.p12 chrX: 31,507,454-31,929,595	DMD
nsv5673683	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 64,940,485-65,336,138 , GRCh38.p12 chr6: 64,230,592-64,626,245	EYS
nsv6308996	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 55,755,399-56,138,712 , GRCh38.p12 chr10: 53,995,639-54,378,952	PCDH15
nsv6309068	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 55,616,925-55,996,701 , GRCh38.p12 chr10: 53,857,165-54,236,941	PCDH15
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
nsv6634681	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 32,663,270-33,038,255 , GRCh38.p12 chrX: 32,645,153-33,020,138	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
nsv6634673	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 31,525,571-31,893,304 , GRCh38.p12 chrX: 31,507,454-31,875,187	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

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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 16273

Page of 814

Number of Variants: 20

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Supplemental Content

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