nstd102 - 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
nsv3875336	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 142,513,049-147,499,105 , GRCh37 chr1: 143,721,526-149,232,481 , GRCh38.p12 chr7: 58,093,723-62,429,627	LOC101060796
nsv6313578	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 69,145,364-70,023,881 , GRCh38.p12 chr7: 69,680,378-70,558,895	AUTS2
nsv3921333	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 68,768,173-69,374,770 , GRCh38 chr7: 69,665,251-70,271,848 , GRCh37 chr7: 69,130,237-69,736,834	AUTS2
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
nsv3897330	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 31,540,244-32,059,446 , GRCh37 chrX: 31,558,361-32,077,563 , NCBI36 chrX: 31,468,282-31,987,484	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
nsv3877736	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 31,533,207-31,983,162 , GRCh38.p12 chrX: 31,515,090-31,965,045	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
nsv5674225	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 162,206,900-162,622,150 , GRCh38.p12 chr6: 161,785,868-162,201,118	PRKN
nsv4769354	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 534,390-935,361 , GRCh38.p12 chrX: 573,655-974,626	SHOX
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
nsv3897255	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 29,147,023-29,533,186 , GRCh38 chrX: 29,128,906-29,515,069 , NCBI36 chrX: 29,056,944-29,443,107	IL1RAPL1
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

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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

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Items: 1 to 20 of 83844

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Number of Variants: 20

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Supplemental Content

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