contrast sensitivity - 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
nsv5672760	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 14,953,179-14,961,841 , GRCh38.p12 chr10: 14,911,180-14,919,842	DCLRE1C
nsv4454495	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 14,939,800-14,945,199 , GRCh37 chr10: 14,981,799-14,987,198	DCLRE1C
nsv7093356	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 14,934,776-14,939,809 , GRCh37.p13 chr10: 14,976,775-14,981,808	DCLRE1C
nsv5381267	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 45,418,966-45,421,117 , GRCh37 chr19: 45,922,224-45,924,375	ERCC1
nsv4454890	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 14,935,443-14,936,613 , GRCh37 chr10: 14,977,442-14,978,612	DCLRE1C
nsv6308988	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 14,977,452-14,978,602 , GRCh38.p12 chr10: 14,935,453-14,936,603	DCLRE1C
nsv3878719	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 14,945,085-14,945,209 , GRCh37 chr10: 14,987,084-14,987,208	DCLRE1C
nsv4683375	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 14,987,094-14,987,198 , GRCh38.p12 chr10: 14,945,095-14,945,199	DCLRE1C
nsv7093869	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 14,991,015-14,991,106 , GRCh38.p12 chr10: 14,949,016-14,949,107	DCLRE1C
nsv6308903	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 14,978,527-14,978,602 , GRCh38.p12 chr10: 14,936,528-14,936,603	DCLRE1C
nsv997178	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chrX: 122,318,096-122,624,766 , GRCh38.p12 chrX: 123,184,243-123,490,915	GRIA3
nsv997137	copy number variation	1	nstd45	human	Pathogenic	GRCh38.p12 chr8: 115,408,496-115,669,028 , GRCh37 chr8: 116,420,724-116,681,255	TRPS1
nsv997145	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chrX: 44,732,421-44,971,857 , GRCh38.p12 chrX: 44,873,175-45,112,612	KDM6A
nsv997104	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chrX: 8,496,915-8,700,228 , GRCh38.p12 chrX: 8,528,874-8,732,187	ANOS1
nsv997235	copy number variation	1	nstd45	human	Pathogenic	GRCh38.p12 chr2: 120,797,291-120,992,653 , GRCh37 chr2: 121,554,867-121,750,229	GLI2
nsv3319002	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chrX: 73,952,691-74,145,287 , GRCh38.p12 chrX: 74,732,856-74,925,452	NEXMIF
nsv997108	copy number variation	1	nstd45	human	Pathogenic	GRCh38.p12 chr8: 60,678,765-60,868,028 , GRCh37 chr8: 61,591,324-61,780,587	CHD7
nsv997153	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chrX: 66,763,874-66,950,461 , GRCh38.p12 chrX: 67,544,032-67,730,619	AR
nsv491564	copy number variation	1	nstd45	human	Pathogenic	GRCh38.p12 chr16: 3,725,055-3,880,120 , GRCh37 chr16: 3,775,056-3,930,121	CREBBP
nsv3318999	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chrX: 40,944,888-41,095,832 , GRCh38.p12 chrX: 41,085,635-41,236,579	USP9X

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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

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Items: 1 to 20 of 402

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Number of Variants: 20

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