dbVar for Gene (Select 215) - 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
nsv6112690	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301	LOC105373176, ZFX-AS1, 2151 more genes
nsv5674189	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 153,001,789-153,009,189 , GRCh38.p12 chrX: 153,736,335-153,743,735	ABCD1
nsv5674182	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 152,991,389-152,991,912 , GRCh38 chrX: 153,725,934-153,726,457	ABCD1
nsv5674083	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 153,002,601-153,002,715 , GRCh38.p12 chrX: 153,737,147-153,737,261	ABCD1
nsv5674082	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 152,990,722-153,009,189 , GRCh38.p12 chrX: 153,725,267-153,743,735	ABCD1
nsv5059979	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 56,469,080-155,233,731 , GRCh38.p12 chrX: 56,442,647-156,004,066	VDAC1P1, LOC105373299, 1364 more genes
nsv4769250	copy number variation	1	nstd201	human		GRCh37 chrX: 96,096,220-155,208,244 , GRCh38.p12 chrX: 96,841,221-155,978,579	, AGTR2, 959 more genes
nsv4769249	copy number variation	1	nstd201	human		GRCh37 chrX: 61,728,816-155,233,846 , GRCh38.p12 chrX: 62,509,346-156,004,181	, ABCB7, 1364 more genes
nsv4728727	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 152,631,130-153,240,286 , GRCh38.p12 chrX: 153,365,672-153,974,835	ARHGAP4, BCAP31, 34 more genes
nsv4728572	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 152,941,302-153,055,639 , GRCh38.p12 chrX: 153,675,847-153,790,184	BCAP31, SRPK3, 6 more genes
nsv4728533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 94,264,404-155,233,731 , GRCh38.p12 chrX: 95,009,405-156,004,066	CT45A10, MIR224, 968 more genes
nsv4728499	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 55,507,789-155,198,481 , GRCh38.p12 chrX: 55,481,356-155,968,816	GABRE, RN7SL325P, 1371 more genes
nsv4685621	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 153,006,133-153,007,471 , GRCh38 chrX: 153,740,679-153,742,017	ABCD1
nsv4685620	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chrX: 122,132,166-155,097,214 , GRCh38.p12 chrX: 122,998,313-155,867,551	ABCD1, AMD1P2, 560 more genes
nsv4683265	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 152,990,712-153,009,199 , GRCh38.p12 chrX: 153,725,257-153,743,745	ABCD1
nsv4682659	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 153,001,556-153,009,199 , GRCh38.p12 chrX: 153,736,102-153,743,745	ABCD1
nsv4681977	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 152,954,010-153,141,311 , GRCh38.p12 chrX: 153,688,555-153,875,856	PLXNB3-AS1, SRPK3, 9 more genes
nsv4681700	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 153,001,556-153,009,189 , GRCh38.p12 chrX: 153,736,102-153,743,735	ABCD1
nsv4681289	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 152,954,010-153,363,142 , GRCh38.p12 chrX: 153,688,555-154,097,685	NAA10, RENBP, 22 more genes
nsv4681160	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 153,001,546-153,009,209 , GRCh38.p12 chrX: 153,736,092-153,743,755	ABCD1

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Number of Variants: 20

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