1-0709-003 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
nsv4379109	copy number variation	1337	nstd173	human		GRCh37 chr20: 1,560,774-1,597,997 , GRCh38.p12 chr20: 1,580,128-1,617,351	SIRPB1
nsv4382555	copy number variation	3	nstd173	human		GRCh37 chr12: 70,175,541-70,205,324 , GRCh38.p12 chr12: 69,781,761-69,811,544	RAB3IP
nsv4377460	copy number variation	116	nstd173	human		GRCh37 chr16: 60,553,311-60,575,074 , GRCh38.p12 chr16: 60,519,407-60,541,170	LOC101927605
nsv4372695	copy number variation	5	nstd173	human		GRCh37 chr6: 49,432,185-49,458,814 , GRCh38.p12 chr6: 49,464,472-49,491,101	CENPQ
nsv4371280	copy number variation	95	nstd173	human		GRCh37 chr1: 72,762,663-72,811,084 , GRCh38.p12 chr1: 72,296,980-72,345,401 , GRCh38.p12 chr1\|NW_018654707.1: 9,247-66,626	RPL31P12, LOC105378797
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
nsv4386470	copy number variation	6	nstd173	human		GRCh37 chr1: 1,397,502-1,429,163 , GRCh38.p12 chr1: 1,462,122-1,493,783	ATAD3B, ATAD3C
nsv4372579	copy number variation	26	nstd173	human		GRCh37 chr5: 180,374,484-180,430,801 , GRCh38.p12 chr5: 180,947,484-181,003,801	BTNL8, LOC100128762, 3 more genes
nsv4374702	copy number variation	95	nstd173	human		GRCh37 chr1: 1,616,990-1,672,603 , GRCh38.p12 chr1: 1,685,551-1,741,164	CDK11A, SLC35E2B, 3 more genes
nsv4367767	copy number variation	8	nstd173	human		GRCh37 chr11: 5,783,327-5,809,230 , GRCh38.p12 chr11: 5,762,097-5,788,000	OR52N1, OR56B2P, 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
nsv4376806	copy number variation	247	nstd173	human		GRCh37 chr12: 11,219,930-11,247,388 , GRCh38.p12 chr12: 11,067,331-11,094,789	PRH1, PRH1-PRR4, 3 more genes
nsv4385215	copy number variation	59	nstd173	human		GRCh37 chr14: 106,880,556-106,922,723 , GRCh38.p12 chr14: 106,424,650-106,466,798 , GRCh38.p12 chr14\|NT_187600.1: 916,329-958,477	IGH, IGHVII-40-1, 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
nsv4368660	copy number variation	868	nstd173	human		GRCh37 chr6: 103,738,197-103,759,824 , GRCh38.p12 chr6: 103,290,322-103,311,949	0
nsv4367764	copy number variation	1	nstd173	human		GRCh37 chr6: 6,780,870-7,153,721 , GRCh38.p12 chr6: 6,780,637-7,153,488	RREB1, BTF3P7, 5 more genes
nsv4372736	copy number variation	43	nstd173	human		GRCh37 chr10: 46,966,534-47,149,411 , GRCh38.p12 chr10: 46,400,352-46,583,083	NPY4R, SYT15-AS1, 5 more genes
nsv4367863	copy number variation	53	nstd173	human		GRCh37 chr4: 69,366,693-69,541,963 , GRCh38.p12 chr4: 68,500,975-68,676,245	UGT2B15, UGT2B29P, 4 more genes
nsv4387566	copy number variation	315	nstd173	human		GRCh37 chr2: 34,701,655-34,727,784 , GRCh38.p12 chr2: 34,476,588-34,502,717	0

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