nstd45 - 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
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

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Result Filters

Object Type

Organism

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Clinical Interpretation

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Sex of Subject

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Subject Phenotype Status

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Items: 1 to 20 of 364

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Number of Variants: 20

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