"nstd45"[study] AND "copy number loss"[variant_type] - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
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
nsv997192	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chr11: 44,117,099-44,266,980 , GRCh38.p12 chr11: 44,095,549-44,245,430	EXT2
nsv997216	copy number variation	1	nstd45	human	Pathogenic	GRCh38.p12 chr15: 67,065,857-67,195,195 , GRCh37 chr15: 67,358,195-67,487,533	SMAD3
nsv3071861	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chrX: 109,917,084-110,039,286 , GRCh38.p12 chrX: 110,673,856-110,796,058	CHRDL1
nsv997142	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chrX: 99,546,642-99,665,271 , GRCh38.p12 chrX: 100,291,644-100,410,273	PCDH19
nsv997107	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chrX: 110,537,007-110,655,460 , GRCh38.p12 chrX: 111,293,779-111,412,232	DCX
nsv997118	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chrX: 20,168,029-20,284,750 , GRCh38.p12 chrX: 20,149,911-20,266,632	RPS6KA3
nsv3170336	copy number variation	1	nstd45	human	Pathogenic	GRCh38.p12 chr2: 182,924,851-183,038,858 , GRCh37 chr2: 183,789,579-183,903,586	NCKAP1
nsv997128	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chrX: 53,963,113-54,071,569 , GRCh38.p12 chrX: 53,936,680-54,045,136	PHF8
nsv997162	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chrX: 149,737,047-149,841,616 , GRCh38.p12 chrX: 150,568,597-150,673,143	MTM1
nsv3170324	copy number variation	1	nstd45	human	Pathogenic	GRCh38.p12 chr2: 60,451,167-60,553,498 , GRCh37 chr2: 60,678,302-60,780,633	BCL11A

dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Subject Phenotype Status

Additional filters

Send to:

Search results

Items: 1 to 20 of 354

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Search details

Recent activity

dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 354

Page of 18

Number of Variants: 20

Page of 18

Supplemental Content

Find related data

Search details

Recent activity