2-1258-002 AND nstd173 - dbVar - NCBI

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Number of Variants: 14

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4386829	copy number variation	19	nstd173	human		GRCh37 chr3: 89,394,591-89,419,367 , GRCh38.p12 chr3: 89,345,441-89,370,217	EPHA3
nsv4380290	copy number variation	32	nstd173	human		GRCh37 chr6: 81,274,336-81,294,386 , GRCh38.p12 chr6: 80,564,619-80,584,669	LOC112267962
nsv4374527	copy number variation	116	nstd173	human		GRCh37 chr2: 98,118,199-98,162,188 , GRCh38.p12 chr2: 97,501,736-97,545,725	ANKRD36B
nsv4377922	copy number variation	2	nstd173	human		GRCh37 chr17: 44,187,492-44,213,649 , GRCh38.p12 chr17: 46,110,126-46,136,283 , GRCh38.p12 chr17\|NT_187663.1: 812,225-838,389	KANSL1
nsv4373446	copy number variation	1	nstd173	human		GRCh37 chr19: 41,338,835-41,380,945 , GRCh38.p12 chr19: 40,832,930-40,875,040	CYP2A6, CYP2A7
nsv4370464	copy number variation	362	nstd173	human		GRCh37 chr11: 4,967,239-4,991,060 , GRCh38.p12 chr11: 4,946,009-4,969,830	OR51A4, OR51A2
nsv4381054	copy number variation	1	nstd173	human		GRCh37 chr5: 156,107,503-156,185,480 , GRCh38.p12 chr5: 156,680,492-156,758,469	LOC105377673, SGCD
nsv4375714	copy number variation	376	nstd173	human		GRCh37 chr4: 69,435,889-69,485,978 , GRCh38.p12 chr4: 68,570,171-68,620,260	UGT2B17, LOC100132651, 1 more genes
nsv4387832	copy number variation	38	nstd173	human		GRCh37 chr12: 11,216,817-11,256,413 , GRCh38.p12 chr12: 11,064,218-11,103,814	TAS2R43, PRH1-TAS2R14, 3 more genes
nsv4370090	copy number variation	36	nstd173	human		GRCh37 chr11: 5,786,008-5,809,230 , GRCh38.p12 chr11: 5,764,778-5,788,000	OR52N5, OR52N1, 1 more genes
nsv4386083	copy number variation	1	nstd173	human		GRCh37 chr19: 55,247,805-55,334,978 , GRCh38.p12 chr19\|NT_187693.1: 718,919-806,092	KIR2DL1, KIR2DL3, 6 more genes
nsv4372694	copy number variation	43	nstd173	human		GRCh37 chr6: 29,841,021-29,921,739 , GRCh38.p12 chr6: 29,873,244-29,953,962	HLA-A, MCCD1P1, 12 more genes
nsv4383655	copy number variation	30	nstd173	human		GRCh37 chr11: 54,965,375-55,009,349 , GRCh38.p12 chr11: 55,197,899-55,241,873	0
nsv4368660	copy number variation	868	nstd173	human		GRCh37 chr6: 103,738,197-103,759,824 , GRCh38.p12 chr6: 103,290,322-103,311,949	0

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