2-1579-003 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
nsv4379505	copy number variation	32	nstd173	human		GRCh37 chr20: 1,557,177-1,590,245 , GRCh38.p12 chr20: 1,576,531-1,609,599	SIRPB1
nsv4378713	copy number variation	50	nstd173	human		GRCh37 chr5: 155,471,684-155,500,768 , GRCh38.p12 chr5: 156,044,674-156,073,758	SGCD
nsv4369656	copy number variation	16	nstd173	human		GRCh37 chr5: 9,901,952-9,926,287 , GRCh38.p12 chr5: 9,901,840-9,926,175	LINC02112
nsv4365093	copy number variation	508	nstd173	human		GRCh37 chr13: 57,758,269-57,778,379 , GRCh38.p12 chr13: 57,184,135-57,204,245	MTCO2P3
nsv4375513	copy number variation	189	nstd173	human		GRCh37 chr1: 72,771,354-72,812,440 , GRCh38.p12 chr1: 72,305,671-72,346,757 , GRCh38.p12 chr1\|NW_018654707.1: 17,938-67,982	LOC105378797
nsv4367391	copy number variation	2	nstd173	human		GRCh37 chr11: 108,586,468-108,815,440 , GRCh38.p12 chr11: 108,715,741-108,944,713	DDX10, CYCSP29
nsv4369328	copy number variation	2	nstd173	human		GRCh37 chr19: 15,777,996-15,820,338 , GRCh38.p12 chr19: 15,667,186-15,709,528	CYP4F10P, CYP4F12
nsv4377132	copy number variation	2	nstd173	human		GRCh37 chr1: 17,594,883-17,619,730 , GRCh38.p12 chr1: 17,268,388-17,293,235 , GRCh38.p12 chr1\|NW_011332688.1: 110,902-138,439	MIR3972, PADI3
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
nsv4370277	copy number variation	687	nstd173	human		GRCh37 chr5: 180,378,754-180,430,789 , GRCh38.p12 chr5: 180,951,754-181,003,789	BTNL8, ARPP19P1, 3 more genes
nsv4382318	copy number variation	21	nstd173	human		GRCh37 chrY: 22,311,731-22,466,082 , GRCh38.p12 chrY: 20,149,845-20,304,196	0
nsv4382768	copy number variation	92	nstd173	human		GRCh37 chr4: 10,209,966-10,240,250 , GRCh38.p12 chr4: 10,208,342-10,238,626	0
nsv4369694	copy number variation	2	nstd173	human		GRCh37 chrX: 3,057,409-3,085,655 , GRCh38.p12 chrX: 3,139,368-3,167,614	0
nsv4371406	copy number variation	8	nstd173	human		GRCh37 chr6: 110,394,605-110,415,232 , GRCh38.p12 chr6: 110,073,402-110,094,029	0
nsv4373366	copy number variation	7	nstd173	human		GRCh37 chr7: 38,322,939-38,370,792 , GRCh38.p12 chr7: 38,283,338-38,331,191	TRGV9, TRG, 7 more genes
nsv4376889	copy number variation	2	nstd173	human		GRCh37 chr14: 22,510,089-22,978,516 , GRCh38.p12 chr14: 22,041,843-22,509,533	TRAJ38, TRAJ61, 70 more genes
nsv4388328	copy number variation	11	nstd173	human		GRCh37 chr7: 142,266,307-142,493,639 , GRCh38.p12 chr7: 142,618,685-142,785,830 , GRCh38.p12 chr7\|NT_187562.1: 656,734-781,128	WBP1LP1, TRBV19, 23 more genes

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