pubic hair OR pubis - 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
nsv7093042	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 108,894,471-108,989,220 , GRCh37.p13 chr2: 109,510,927-109,605,676	EDAR
nsv4682254	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 77,238,734-77,312,616 , GRCh38.p12 chrX: 77,983,238-78,057,119	ATP7A
nsv5381794	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 3,784,414-3,821,324 , GRCh38.p12 chr16: 3,734,413-3,771,323	CREBBP
nsv5674217	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 77,227,108-77,258,743 , GRCh38.p12 chrX: 77,971,611-78,003,246	ATP7A
nsv7097088	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 7,567,563-7,584,301 , GRCh38.p12 chr6: 7,567,330-7,584,068	DSP
nsv3886689	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 7,570,650-7,586,131 , GRCh38 chr6: 7,570,417-7,585,898	DSP
nsv4682590	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 7,570,660-7,586,121 , GRCh38.p12 chr6: 7,570,427-7,585,888	DSP
nsv1398543	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 108,896,907-108,906,334 , GRCh37 chr2: 109,513,363-109,522,790	EDAR
nsv6315034	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr3: 185,231,236-185,236,525 , GRCh38 chr3: 185,513,448-185,518,737	LIPH
nsv6312410	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 7,583,161-7,587,903 , GRCh38.p12 chr6: 7,582,928-7,587,670	DSP
nsv5674021	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 7,565,582-7,569,583 , GRCh38.p12 chr6: 7,565,349-7,569,350	DSP
nsv6313468	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 77,264,993-77,268,389 , GRCh38.p12 chrX: 78,009,496-78,012,892	ATP7A
nsv6313381	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 77,275,721-77,279,056 , GRCh38.p12 chrX: 78,020,224-78,023,559	ATP7A
nsv7097089	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 7,582,855-7,586,131 , GRCh38.p12 chr6: 7,582,622-7,585,898	DSP
nsv7097847	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 7,582,865-7,586,121 , GRCh38.p12 chr6: 7,582,632-7,585,888	DSP
nsv3881467	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 108,910,426-108,912,698 , GRCh37 chr2: 109,526,882-109,529,154	EDAR
nsv6313467	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 77,243,718-77,245,474 , GRCh38.p12 chrX: 77,988,222-77,989,978	ATP7A
nsv5674170	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 77,270,139-77,271,398 , GRCh38.p12 chrX: 78,014,642-78,015,901	ATP7A
nsv7098550	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 77,300,947-77,302,067 , GRCh38.p12 chrX: 78,045,450-78,046,570	ATP7A
nsv4348716	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 77,244,108-77,244,998 , GRCh38.p12 chrX: 77,988,612-77,989,502	ATP7A

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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 75

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Number of Variants: 20

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