240259S AND nstd173 - dbVar - NCBI

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Items: 18

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Number of Variants: 18

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4376255	copy number variation	343	nstd173	human		GRCh37 chr2: 98,118,199-98,162,176 , GRCh38.p12 chr2: 97,501,736-97,545,713	ANKRD36B
nsv4379737	copy number variation	349	nstd173	human		GRCh37 chr1: 169,216,099-169,241,765 , GRCh38.p12 chr1: 169,246,861-169,272,527	NME7
nsv4372752	copy number variation	1	nstd173	human		GRCh37 chr11: 18,941,182-18,961,339 , GRCh38.p12 chr11: 18,919,635-18,939,792	MRGPRX1
nsv4376456	copy number variation	1782	nstd173	human		GRCh37 chr8: 39,246,772-39,386,964 , GRCh38.p12 chr8: 39,389,253-39,529,445	ADAM5, ADAM3A
nsv4386078	copy number variation	2	nstd173	human		GRCh37 chr2: 112,132,624-112,188,518 , GRCh38.p12 chr2: 111,375,047-111,430,941	PAFAH1B1P2, MIR4435-2HG
nsv4384457	copy number variation	635	nstd173	human		GRCh37 chr11: 55,374,031-55,453,008 , GRCh38.p12 chr11: 55,606,555-55,685,532	OR4P1P, OR4C6, 3 more genes
nsv4378623	copy number variation	41	nstd173	human		GRCh37 chr6: 254,254-294,923 , GRCh38.p12 chr6: 254,254-294,923	, DUSP22, 1 more genes
nsv4375662	copy number variation	272	nstd173	human		GRCh37 chr11: 5,783,910-5,809,230 , GRCh38.p12 chr11: 5,762,680-5,788,000	OR52N1, OR56B2P, 1 more genes
nsv4366691	copy number variation	623	nstd173	human		GRCh37 chr4: 69,435,901-69,485,978 , GRCh38.p12 chr4: 68,570,183-68,620,260	UGT2B17, LOC100422402, 1 more genes
nsv4365609	copy number variation	38	nstd173	human		GRCh37 chrY: 22,311,731-22,489,344 , GRCh38.p12 chrY: 20,149,845-20,327,458	0
nsv4365794	copy number variation	17	nstd173	human		GRCh37 chr14: 107,158,227-107,179,594 , GRCh38.p12 chr14: 106,702,210-106,771,352	IGH, IGHV1-69-2, 6 more genes
nsv4382973	copy number variation	317	nstd173	human		GRCh37 chr5: 180,378,754-180,442,428 , GRCh38.p12 chr5: 180,951,754-181,015,428	BTNL3, LOC100128762, 4 more genes
nsv4385178	copy number variation	7	nstd173	human		GRCh37 chr17: 44,162,713-44,784,639 , GRCh38.p12 chr17: 46,085,347-46,707,273 , GRCh38.p12 chr17\|NT_187663.1: 787,448-1,226,699	FAM215B, RN7SL199P, 14 more genes
nsv4379056	copy number variation	1	nstd173	human		GRCh37 chr14: 22,419,237-23,002,684 , GRCh38.p12 chr14: 21,951,014-22,533,736	TRAJ53, TRAJ30, 101 more genes
nsv4370124	copy number variation	182	nstd173	human		GRCh37 chr7: 142,266,307-142,493,638 , GRCh38.p12 chr7: 142,618,685-142,785,829 , GRCh38.p12 chr7\|NT_187562.1: 656,734-781,128	TRBV27, TRBV21-1, 23 more genes
nsv4381873	copy number variation	40	nstd173	human		GRCh37 chr14: 106,536,991-106,692,891 , GRCh38.p12 chr14: 106,112,755-106,236,281 , GRCh38.p12 chr14\|NT_187600.1: 580,524-704,050	IGHV3-19, LOC105370700, 17 more genes
nsv4375592	copy number variation	3	nstd173	human		GRCh37 chr7: 38,290,714-38,405,084 , GRCh38.p12 chr7: 38,251,113-38,365,483	TRGV5P, TRGJP, 22 more genes
nsv4376482	copy number variation	1	nstd173	human		GRCh37 chr3: 135,312,613-135,386,484 , GRCh38.p12 chr3: 135,593,771-135,667,642	0

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