16-1002-001 AND nstd173 - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
nsv4379319	copy number variation	5	nstd173	human	GRCh37 chr1: 73,012,023-73,086,201 , GRCh38.p12 chr1: 72,546,340-72,620,518	LOC105378797
nsv4366806	copy number variation	4	nstd173	human	GRCh37 chr11: 49,703,188-49,757,670 , GRCh38.p12 chr11: 49,681,636-49,736,118 , GRCh38.p12 chr11\|NW_019805495.1: 145,816-200,267	GRM5P1
nsv4382938	copy number variation	14	nstd173	human	GRCh37 chr20: 1,560,530-1,597,997 , GRCh38.p12 chr20: 1,579,884-1,617,351	SIRPB1
nsv4383572	copy number variation	17	nstd173	human	GRCh37 chr4: 161,952,214-162,003,219 , GRCh38.p12 chr4: 161,031,062-161,082,067	LOC105377514
nsv4379155	copy number variation	63	nstd173	human	GRCh37 chr3: 173,239,853-173,289,847 , GRCh38.p12 chr3: 173,522,063-173,572,057	NLGN1
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
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
nsv4384822	copy number variation	80	nstd173	human	GRCh37 chr7: 43,361-81,400 , GRCh38.p12 chr7: 43,361-81,400 , GRCh38.p12 chr7\|NT_187558.1: 1-37,499 , GRCh38.p12 chr7\|NT_187653.1: 35,682-73,721	LOC105375113, LOC101929756
nsv4377863	copy number variation	57	nstd173	human	GRCh37 chr19: 52,131,800-52,157,402 , GRCh38.p12 chr19: 51,628,547-51,654,149	RPL7P51, SIGLEC14, 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
nsv4371739	copy number variation	1	nstd173	human	GRCh37 chr15: 43,907,776-44,007,537 , GRCh38.p12 chr15: 43,615,578-43,715,339	CATSPER2, STRC, 7 more genes
nsv4375049	copy number variation	38	nstd173	human	GRCh37 chrX: 111,718,452-111,751,443 , GRCh38.p12 chrX: 112,475,224-112,508,215	0
nsv4367610	copy number variation	2	nstd173	human	GRCh37 chr10: 135,252,179-135,377,277 , GRCh38.p12 chr10: 133,438,675-133,563,773	CYP2E1, LOC105378575, 5 more genes
nsv4387967	copy number variation	1	nstd173	human	GRCh37 chr7: 142,427,828-142,491,993 , GRCh38.p12 chr7: 142,720,004-142,784,183 , GRCh38.p12 chr7\|NT_187562.1: 734,718-781,128	TRBV29-1, PRSS3P1, 7 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
nsv4386206	copy number variation	10	nstd173	human	GRCh37 chr14: 22,510,089-22,960,757 , GRCh38.p12 chr14: 22,041,843-22,491,770	, TRAV36DV7, 55 more genes
nsv4371117	copy number variation	49	nstd173	human	GRCh37 chr7: 38,294,088-38,394,857 , GRCh38.p12 chr7: 38,254,487-38,355,256	TRGVA, TRGC1, 19 more genes
nsv4370756	copy number variation	114	nstd173	human	GRCh37 chr11: 54,701,632-54,788,759 , GRCh38.p12 chr11: 54,934,156-55,021,283	0
nsv4370845	copy number variation	1	nstd173	human	GRCh37 chr14: 106,880,556-106,951,724 , GRCh38.p12 chr14: 106,424,650-106,495,710 , GRCh38.p12 chr14\|NT_187600.1: 916,329-987,389	IGHV3-42, IGHV7-40, 10 more genes
nsv4368473	copy number variation	289	nstd173	human	GRCh37 chr22: 42,918,351-42,943,641 , GRCh38.p12 chr22: 42,522,345-42,547,635	0

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Number of Variants: 20

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