dbVar for Gene (Select 100500915) - 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
nsv7148231	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 32,536,377-32,771,300 , GRCh37.p13 chrX: 32,554,494-32,789,417	DMD, MIR548F5, 1 more genes
nsv7148144	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 32,216,792-33,041,819 , GRCh37.p13 chrX: 32,234,909-33,059,936	MIR548F5, TBCAP1, 2 more genes
nsv7148140	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 23,730,430-32,849,918 , GRCh37.p13 chrX: 23,748,547-32,868,035	ARX, LOC107985632, 85 more genes
nsv7137157	inversion	1	nstd234	human		GRCh37 chrX: 31,626,542-82,320,140 , GRCh38.p12 chrX: 31,608,425-83,065,132	ABCB7, ACTG1P10, 775 more genes
nsv7137063	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409	RN7SL581P, HMGB1P32, 2151 more genes
nsv7136972	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 32,519,960-33,229,674 , GRCh38.p12 chrX: 32,501,843-33,211,557	DMD, MIR3915, 2 more genes
nsv7098960	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 32,398,798-32,827,609 , GRCh38.p12 chrX: 32,380,681-32,809,492	MIR548F5, MIR3915, 1 more genes
nsv7098861	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 32,563,274-32,717,411 , GRCh38.p12 chrX: 32,545,157-32,699,294	DMD, MIR548F5, 1 more genes
nsv7098736	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chrX: 32,408,299-32,834,584 , GRCh38.p12 chrX: 32,390,182-32,816,467	DMD, MIR548F5, 1 more genes
nsv7098651	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 32,583,799-32,663,289 , GRCh38.p12 chrX: 32,565,682-32,645,172	MIR3915, DMD, 1 more genes
nsv7098650	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 32,563,256-32,717,430 , GRCh38.p12 chrX: 32,545,139-32,699,313	DMD, MIR3915, 1 more genes
nsv7098649	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 32,536,105-32,614,013 , GRCh38.p12 chrX: 32,517,988-32,595,896	DMD, MIR3915
nsv7098648	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 32,509,374-32,663,289 , GRCh38.p12 chrX: 32,491,257-32,645,172	DMD, MIR548F5, 1 more genes
nsv7098647	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 32,503,016-32,756,908 , GRCh38.p12 chrX: 32,484,899-32,738,791	DMD, MIR548F5, 1 more genes
nsv7098643	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 32,456,338-32,756,908 , GRCh38.p12 chrX: 32,438,221-32,738,791	DMD, MIR548F5, 1 more genes
nsv7098640	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 32,360,197-32,717,430 , GRCh38.p12 chrX: 32,342,080-32,699,313	MIR548F5, MIR3915, 1 more genes
nsv7098638	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 31,983,146-32,756,908 , GRCh38.p12 chrX: 31,965,029-32,738,791	NPM1P8, MIR3915, 3 more genes
nsv7098637	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 31,947,693-32,669,194 , GRCh38.p12 chrX: 31,929,576-32,651,077	NPM1P8, MIR3915, 3 more genes
nsv7098636	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 31,854,815-32,867,957 , GRCh38.p12 chrX: 31,836,698-32,849,840	NPM1P8, MIR3915, 3 more genes
nsv7098624	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 31,241,144-33,229,429 , GRCh38.p12 chrX: 31,223,027-33,211,312	DMD, TBCAP1, 5 more genes

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Organism

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 546

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Number of Variants: 20

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