sample62 AND nstd145 - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
nsv3113934	copy number variation	6	nstd145	human	GRCh37 chr16: 55,797,365-55,832,503 , GRCh38.p12 chr16: 55,763,453-55,798,591	CES1P1
nsv3116503	copy number variation	1	nstd145	human	GRCh37 chr7: 141,762,093-141,785,344 , GRCh38.p12 chr7: 142,062,293-142,085,544 , GRCh38.p12 chr7\|NT_187562.1: 24,173-47,424	MGAM
nsv3114057	copy number variation	160	nstd145	human	GRCh37 chr19: 52,134,789-52,148,550 , GRCh38.p12 chr19: 51,631,536-51,645,297	SIGLEC14
nsv3112836	copy number variation	1	nstd145	human	GRCh37 chr4: 138,086,847-138,099,949 , GRCh38.p12 chr4: 137,165,693-137,178,795	LINC02511
nsv3115831	copy number variation	1	nstd145	human	GRCh37 chr9: 87,514,514-87,525,509 , GRCh38.p12 chr9: 84,899,599-84,910,594	NTRK2
nsv3116140	copy number variation	45	nstd145	human	GRCh37 chr4: 21,369,066-21,376,838 , GRCh38.p12 chr4: 21,367,443-21,375,215	KCNIP4
nsv3111700	copy number variation	32	nstd145	human	GRCh37 chr3: 192,875,554-192,883,085 , GRCh38.p12 chr3: 193,157,765-193,165,296	VEZF1P1
nsv3114687	copy number variation	1	nstd145	human	GRCh37 chr7: 39,260,897-39,268,257 , GRCh38.p12 chr7: 39,221,298-39,228,658	POU6F2
nsv3113837	copy number variation	1	nstd145	human	GRCh37 chr10: 53,087,850-53,094,401 , GRCh38.p12 chr10: 51,328,090-51,334,641	PRKG1
nsv3118262	copy number variation	3	nstd145	human	GRCh37 chr8: 593,869-599,002 , GRCh38.p12 chr8: 643,869-649,002	ERICH1
nsv3115596	copy number variation	45	nstd145	human	GRCh37 chr3: 148,964,056-148,969,130 , GRCh38.p12 chr3: 149,246,269-149,251,343	CPHL1P
nsv3112456	copy number variation	1	nstd145	human	GRCh37 chr18: 12,307,234-12,311,813 , GRCh38.p12 chr18: 12,307,235-12,311,814	TUBB6
nsv3110593	copy number variation	88	nstd145	human	GRCh37 chr8: 40,774,871-40,779,295 , GRCh38.p12 chr8: 40,917,352-40,921,776	LOC105379389
nsv3115681	copy number variation	1	nstd145	human	GRCh37 chr15: 85,239,207-85,243,110 , GRCh38.p12 chr15: 84,695,976-84,699,879	SEC11A
nsv3117382	copy number variation	1	nstd145	human	GRCh37 chr5: 12,811,668-12,815,461 , GRCh38.p12 chr5: 12,811,556-12,815,349	LOC105374657
nsv3113712	copy number variation	2	nstd145	human	GRCh37 chr16: 78,486,060-78,489,084 , GRCh38.p12 chr16: 78,452,163-78,455,187	WWOX
nsv3114457	copy number variation	1	nstd145	human	GRCh37 chr22: 45,753,922-45,756,766 , GRCh38.p12 chr22: 45,358,042-45,360,886	SMC1B
nsv3115541	copy number variation	1	nstd145	human	GRCh37 chr11: 113,744,023-113,746,803 , GRCh38.p12 chr11: 113,873,301-113,876,081	USP28
nsv3117234	copy number variation	1	nstd145	human	GRCh37 chr3: 77,396,342-77,398,772 , GRCh38.p12 chr3: 77,347,191-77,349,621	ROBO2
nsv3110350	copy number variation	1	nstd145	human	GRCh37 chr2: 176,995,511-176,997,260 , GRCh38.p12 chr2: 176,130,783-176,132,532	HOXD8

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Subject Phenotype Status

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Items: 1 to 20 of 54

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Number of Variants: 20

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