211608 AND nstd173 - dbVar - NCBI

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Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4386852	copy number variation	127	nstd173	human		GRCh37 chr8: 137,677,896-137,862,435 , GRCh38.p12 chr8: 136,665,653-136,850,192	LINC02055
nsv4384091	copy number variation	77	nstd173	human		GRCh37 chr11: 49,710,704-49,746,720 , GRCh38.p12 chr11: 49,689,152-49,725,168 , GRCh38.p12 chr11\|NW_019805495.1: 153,334-179,145	GRM5P1
nsv4370897	copy number variation	108	nstd173	human		GRCh37 chr13: 57,758,269-57,778,367 , GRCh38.p12 chr13: 57,184,135-57,204,233	MTCO2P3
nsv4365971	copy number variation	432	nstd173	human		GRCh37 chr1: 248,753,196-248,795,289 , GRCh38.p12 chr1: 248,589,895-248,631,988	OR2T10, OR2T11
nsv4375141	copy number variation	7	nstd173	human		GRCh37 chr8: 39,230,324-39,386,964 , GRCh38.p12 chr8: 39,372,805-39,529,445	ADAM5, ADAM3A
nsv4386667	copy number variation	4	nstd173	human		GRCh37 chrY: 24,804,259-24,993,248 , GRCh38.p12 chrY: 22,658,112-22,847,101	LOC107987348, FAM8A10P, 1 more genes
nsv4383263	copy number variation	11	nstd173	human		GRCh37 chr6: 253,308-387,482 , GRCh38.p12 chr6: 253,308-387,482	DUSP22, , 1 more genes
nsv4370401	copy number variation	2	nstd173	human		GRCh37 chrY: 27,653,382-27,778,829 , GRCh38.p12 chrY: 25,507,235-25,632,682	CDY19P, USP9YP36, 3 more genes
nsv4367271	copy number variation	561	nstd173	human		GRCh37 chr11: 5,786,020-5,809,230 , GRCh38.p12 chr11: 5,764,790-5,788,000	OR56B2P, OR52N1, 1 more genes
nsv4368193	copy number variation	62	nstd173	human		GRCh37 chr11: 55,402,801-55,442,305 , GRCh38.p12 chr11: 55,635,325-55,674,829	OR4P4, OR4V1P, 2 more genes
nsv4378793	copy number variation	2	nstd173	human		GRCh37 chrY: 27,038,404-27,488,471 , GRCh38.p12 chrY: 24,892,257-25,342,324	RBMY2YP, TTTY17C, 11 more genes
nsv4367390	copy number variation	2	nstd173	human		GRCh37 chrY: 26,501,385-26,921,753 , GRCh38.p12 chrY: 24,355,238-24,775,606	TRIM60P10Y, TRIM60P5Y, 11 more genes
nsv4374159	copy number variation	3	nstd173	human		GRCh37 chrY: 25,842,939-26,184,108 , GRCh38.p12 chrY: 23,696,792-24,037,961	ELOCP10, XKRYP3, 18 more genes
nsv4379976	copy number variation	1	nstd173	human		GRCh37 chrY: 27,792,022-28,113,644 , GRCh38.p12 chrY: 25,645,875-25,967,497	RAB9AP3, RNU1-40P, 19 more genes
nsv4378481	copy number variation	186	nstd173	human		GRCh37 chr2: 4,208,245-4,234,699 , GRCh38.p12 chr2: 4,160,655-4,187,109	0
nsv4382392	copy number variation	421	nstd173	human		GRCh37 chr3: 65,185,849-65,210,375 , GRCh38.p12 chr3: 65,200,174-65,224,700	0
nsv4374107	copy number variation	20	nstd173	human		GRCh37 chr14: 22,410,620-22,974,280 , GRCh38.p12 chr14: 21,942,429-22,505,293	TRDJ3, TRAJ43, 75 more genes
nsv4376301	copy number variation	4	nstd173	human		GRCh37 chr7: 142,331,234-142,499,697 , GRCh38.p12 chr7: 142,623,720-142,802,013 , GRCh38.p12 chr7\|NT_187562.1: 656,734-781,128	TRBJ2-1, TRBVB, 36 more genes
nsv4368801	copy number variation	4	nstd173	human		GRCh37 chr7: 38,286,515-38,394,857 , GRCh38.p12 chr7: 38,246,914-38,355,256	TRGV4, TRG, 21 more genes

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