222688 AND nstd173 - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
nsv4388274	copy number variation	3	nstd173	human	GRCh37 chr14: 46,841,642-46,878,299 , GRCh38.p12 chr14: 46,372,439-46,409,096	LINC00871
nsv4368218	copy number variation	6	nstd173	human	GRCh37 chr2: 66,178,510-66,200,547 , GRCh38.p12 chr2: 65,951,376-65,973,413	LINC02934
nsv4368434	copy number variation	189	nstd173	human	GRCh37 chr1: 72,771,366-72,812,440 , GRCh38.p12 chr1: 72,305,683-72,346,757 , GRCh38.p12 chr1\|NW_018654707.1: 17,950-67,982	LOC105378797
nsv4381042	copy number variation	6	nstd173	human	GRCh37 chr12: 2,235,941-2,258,103 , GRCh38.p12 chr12: 2,126,775-2,148,937 , GRCh38.p12 chr12\|NW_018654718.1: 468,919-491,081	LOC107984131, CACNA1C
nsv4371354	copy number variation	1	nstd173	human	GRCh37 chr5: 15,297,739-15,402,008 , GRCh38.p12 chr5: 15,297,630-15,401,899	LOC100270647, MARK2P5
nsv4381433	copy number variation	68	nstd173	human	GRCh37 chr1: 196,827,842-196,877,049 , GRCh38.p12 chr1: 196,858,712-196,907,919	LOC100996886, CFHR4
nsv4386727	copy number variation	5	nstd173	human	GRCh37 chr15: 24,371,261-24,504,770 , GRCh38.p12 chr15: 24,126,114-24,259,623	PWRN2, LOC105370732, 1 more genes
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
nsv4370631	copy number variation	136	nstd173	human	GRCh37 chr11: 5,787,573-5,809,230 , GRCh38.p12 chr11: 5,766,343-5,788,000	OR52N1, OR56B2P, 1 more genes
nsv4383173	copy number variation	8	nstd173	human	GRCh37 chr17: 44,187,492-44,292,676 , GRCh38.p12 chr17: 46,110,126-46,215,310 , GRCh38.p12 chr17\|NT_187663.1: 812,225-917,483	KANSL1, KANSL1-AS1, 1 more genes
nsv4382082	copy number variation	609	nstd173	human	GRCh37 chr11: 55,374,019-55,442,305 , GRCh38.p12 chr11: 55,606,543-55,674,829	OR4C6, OR4P4, 2 more genes
nsv4371991	copy number variation	196	nstd173	human	GRCh37 chr19: 20,596,118-20,720,705 , GRCh38.p12 chr19: 20,413,312-20,537,899	ZNF826P, ZNF737, 4 more genes
nsv4369919	copy number variation	116	nstd173	human	GRCh37 chr14: 106,530,472-106,667,035 , GRCh38.p12 chr14: 106,074,229-106,210,392 , GRCh38.p12 chr14\|NT_187600.1: 541,998-678,161	IGHV1-18, IGHV3-20, 17 more genes
nsv4371199	copy number variation	115	nstd173	human	GRCh37 chr2: 52,738,983-52,790,493 , GRCh38.p12 chr2: 52,511,845-52,563,355	0
nsv4381531	copy number variation	237	nstd173	human	GRCh37 chr2: 34,701,643-34,737,163 , GRCh38.p12 chr2: 34,476,576-34,512,096	0
nsv4384501	copy number variation	242	nstd173	human	GRCh37 chr16: 19,945,795-19,965,942 , GRCh38.p12 chr16: 19,934,473-19,954,620	0
nsv4368173	copy number variation	30	nstd173	human	GRCh37 chr5: 180,374,484-180,442,428 , GRCh38.p12 chr5: 180,947,484-181,015,428	RNU6-1036P, BTNL3, 4 more genes
nsv4385793	copy number variation	9	nstd173	human	GRCh37 chr14: 22,481,528-22,974,280 , GRCh38.p12 chr14: 22,013,289-22,505,293	TRDJ3, TRAJ43, 68 more genes
nsv4371086	copy number variation	24	nstd173	human	GRCh37 chr7: 38,293,950-38,405,084 , GRCh38.p12 chr7: 38,254,349-38,365,483	TRGJP1, TRGV2, 21 more genes
nsv4387573	copy number variation	172	nstd173	human	GRCh37 chr11: 54,701,632-54,757,928 , GRCh38.p12 chr11: 54,934,156-54,990,452	0

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Number of Variants: 20

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