OAT_30 AND nstd53 - dbVar - NCBI

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Items: 12

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Number of Variants: 12

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv869731	copy number variation	10	nstd53	human		GRCh38.p12 chr8: 136,667,427-136,850,282 , NCBI36 chr8: 137,748,852-137,931,707 , GRCh37.p13 chr8: 137,679,670-137,862,525	LINC02055
nsv870374	copy number variation	79	nstd53	human		NCBI36 chr1: 72,541,502-72,589,682 , GRCh38.p12 chr1: 72,303,231-72,351,411 , GRCh37.p13 chr1: 72,768,914-72,817,094 , GRCh38.p12 chr1\|NW_018654707.1: 15,498-72,636	LOC105378797
nsv870180	copy number variation	11	nstd53	human		NCBI36 chr16: 54,356,757-54,390,012 , GRCh38.p12 chr16: 55,765,344-55,798,599 , GRCh37.p13 chr16: 55,799,256-55,832,511	CES1P1
nsv870018	copy number variation	68	nstd53	human		NCBI36 chr20: 1,511,774-1,528,899 , GRCh37.p13 chr20: 1,563,774-1,580,899 , GRCh38.p12 chr20: 1,583,128-1,600,253	SIRPB1
nsv870138	copy number variation	2	nstd53	human		GRCh38.p12 chr2: 110,079,439-110,226,067 , NCBI36 chr2: 110,194,305-110,340,933 , GRCh37.p13 chr2: 110,837,016-110,983,644	NPHP1, MALL, 3 more genes
nsv870009	copy number variation	36	nstd53	human		GRCh37.p13 chr3: 195,354,183-195,457,709 , GRCh38.p12 chr3: 195,627,312-195,730,838 , NCBI36 chr3: 196,835,472-196,943,380 , GRCh38.p12 chr3\|NT_187649.1: 63,861-139,787 , GRCh38.p12 chr3\|NT_187688.1: 63,861-140,349 , GRCh38.p12 chr3\|NT_187690.1: 63,868-141,061 , GRCh38.p12 chr3\|NT_187691.1: 64,038-142,498 , GRCh38.p12 chr3\|NT_187678.1: 65,206-143,431 , GRCh38.p12 chr3\|NT_187689.1: 23,110-101,335 , GRCh38.p12 chr3\|NT_187532.1: 23,110-101,335	MUC20, MIR570HG, 7 more genes
nsv869577	copy number variation	64	nstd53	human		NCBI36 chr15: 18,867,344-19,943,194 , GRCh38.p12 chr15: 20,402,077-22,153,879 , GRCh37.p13 chr15: 20,607,330-22,441,830	NBEAP1, OR4H6P, 78 more genes
nsv870097	copy number variation	1	nstd53	human		NCBI36 chr14: 105,597,311-105,902,383 , GRCh38.p12 chr14: 106,070,018-106,375,407 , GRCh37.p13 chr14: 106,526,266-106,831,338 , GRCh38.p12 chr14\|NT_187600.1: 502,910-1,214,078	IGH, IGHVIV-44-1, 113 more genes
nsv870413	copy number variation	41	nstd53	human		GRCh38.p12 chr2: 34,472,710-34,513,110 , NCBI36 chr2: 34,551,281-34,591,681 , GRCh37.p13 chr2: 34,697,777-34,738,177	0
nsv870142	copy number variation	3	nstd53	human		NCBI36 chr1: 16,704,572-17,154,206 , GRCh38.p12 chr1: 16,505,490-16,955,124 , GRCh37.p13 chr1: 16,831,985-17,281,619	RNU1-4, TRE-TTC3-1, 34 more genes
nsv870132	copy number variation	1	nstd53	human		NCBI36 chr16: 34,329,577-34,634,686 , GRCh38.p12 chr16: 35,237,705-35,542,814 , GRCh37.p13 chr16: 34,472,076-34,777,185	FRG2DP, LINC01566, 26 more genes
nsv869808	copy number variation	12	nstd53	human		NCBI36 chr14: 106,219,843-106,256,498 , GRCh38.p12 chr14: 106,692,781-106,777,214 , GRCh37.p13 chr14: 107,148,798-107,185,453	IGH, IGHVIII-67-4, 9 more genes

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OAT_30 AND nstd53 (13)
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