SP52328 AND nstd71 - dbVar - NCBI

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Items: 16

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Number of Variants: 16

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv884822	copy number variation	2547	nstd71	human		NCBI36 chr6: 32,560,168-32,593,470 , GRCh37.p13 chr6: 32,452,190-32,485,492 , GRCh38.p12 chr6: 32,484,413-32,517,715	HLA-DRB5
nsv909839	copy number variation	966	nstd71	human		NCBI36 chr18: 64,895,268-64,909,808 , GRCh37.p13 chr18: 66,744,288-66,758,828 , GRCh38.p12 chr18: 69,077,051-69,091,591	CCDC102B
nsv885567	copy number variation	32	nstd71	human		NCBI36 chr6: 32,711,738-32,732,638 , GRCh37.p13 chr6: 32,603,760-32,624,660 , GRCh38.p12 chr6: 32,635,983-32,656,883	, HLA-DQA1
nsv911382	copy number variation	222	nstd71	human		NCBI36 chr19: 20,413,668-20,520,617 , GRCh37.p13 chr19: 20,621,828-20,728,777 , GRCh37.p13 chr19\|NW_003571053.2: 356,275-463,224 , GRCh38.p12 chr19: 20,439,022-20,545,971	BNIP3P23, LOC105372317, 2 more genes
nsv882084	copy number variation	25	nstd71	human		NCBI36 chr5: 70,232,726-70,300,876 , GRCh37.p13 chr5: 70,196,970-70,265,120 , GRCh38.p12 chr5: 70,901,143-70,969,293	SERF1A, NAIP, 2 more genes
nsv883570	copy number variation	167	nstd71	human		NCBI36 chr6: 29,957,666-29,972,182 , GRCh37.p13 chr6: 29,849,687-29,864,203 , GRCh38.p12 chr6: 29,881,910-29,896,426	HLA-T, HCG4P7, 1 more genes
nsv883931	copy number variation	35	nstd71	human		NCBI36 chr6: 29,989,443-30,003,207 , GRCh37.p13 chr6\|NT_167246.1: 1,175,640-1,189,435 , GRCh37.p13 chr6: 29,881,464-29,895,228 , GRCh38.p12 chr6: 29,913,687-29,927,451 , GRCh38.p12 chr6\|NT_167246.2: 1,170,020-1,183,815	HCG4B, HLA-K, 1 more genes
nsv883811	copy number variation	81	nstd71	human		NCBI36 chr6: 29,978,470-29,988,619 , GRCh37.p13 chr6\|NT_167246.1: 1,164,662-1,174,816 , GRCh37.p13 chr6: 29,870,491-29,880,640 , GRCh38.p12 chr6\|NT_167246.2: 1,159,042-1,169,196 , GRCh38.p12 chr6: 29,902,714-29,912,863	HLA-A, DDX39BP1, 2 more genes
nsv894691	copy number variation	1	nstd71	human		NCBI36 chr10: 1-122,330 , GRCh37.p13 chr: NaN-NaN , GRCh38.p12 chr10: 14,062-86,390	IL9RP2, TUBB8, 1 more genes
nsv906916	copy number variation	10	nstd71	human		NCBI36 chr16: 74,086,012-74,136,734 , GRCh37.p13 chr16: 75,528,511-75,579,233 , GRCh38.p12 chr16: 75,494,613-75,545,335	CHST5, TMEM231P1, 2 more genes
nsv884573	copy number variation	5	nstd71	human		NCBI36 chr6: 32,058,245-32,111,860 , GRCh37.p13 chr6\|NT_167247.1: 3,355,526-3,383,726 , GRCh37.p13 chr6\|NT_167245.1: 3,235,847-3,270,782 , GRCh37.p13 chr6: 31,950,266-32,003,881 , GRCh37.p13 chr6\|NT_167249.1: 3,282,976-3,336,592 , GRCh38.p12 chr6\|NT_167247.2: 3,349,941-3,378,141 , GRCh38.p12 chr6\|NT_167249.2: 3,283,678-3,337,294 , GRCh38.p12 chr6\|NT_167245.2: 3,230,262-3,265,197 , GRCh38.p12 chr6: 31,982,489-32,036,104	TNXA, STK19B, 5 more genes
nsv906465	copy number variation	10	nstd71	human		NCBI36 chr16: 32,474,045-32,511,911 , GRCh37.p13 chr16: 32,566,544-32,604,410 , GRCh38.p12 chr16: 32,555,223-32,593,089	0
nsv906130	copy number variation	1	nstd71	human		NCBI36 chr16: 32,437,238-32,445,732 , GRCh37.p13 chr16: 32,529,737-32,538,231 , GRCh38.p12 chr16: 32,518,416-32,526,910	0
nsv884256	copy number variation	61	nstd71	human		NCBI36 chr6: 31,388,306-31,396,472 , GRCh37.p13 chr6: 31,280,327-31,288,493 , GRCh37.p13 chr6\|NT_167246.1: 2,627,146-2,631,393 , GRCh37.p13 chr6\|NT_167249.1: 2,614,037-2,622,207 , GRCh38.p12 chr6\|NT_167246.2: 2,621,526-2,625,775 , GRCh38.p12 chr6: 31,312,550-31,320,716 , GRCh38.p12 chr6\|NT_167249.2: 2,614,739-2,622,909	0
nsv881830	copy number variation	2	nstd71	human		NCBI36 chr5: 69,280,018-69,440,843 , GRCh37.p13 chr5: 69,244,262-69,405,087 , GRCh38.p12 chr5: 69,948,435-70,109,260 , GRCh38.p12 chr5\|NT_187651.1: 243,313-334,610	GUSBP15, LOC105369228, 6 more genes
nsv873442	copy number variation	1	nstd71	human		NCBI36 chr1: 245,963,172-246,417,399 , GRCh37.p13 chr1: 247,896,549-248,350,776 , GRCh38.p12 chr1: 247,733,247-248,187,474	CLK3P2, OR2L13, 27 more genes

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