2-1618-001 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
nsv4385735	copy number variation	9	nstd173	human		GRCh37 chr4: 34,779,032-34,835,587 , GRCh38.p12 chr4: 34,777,410-34,833,965 , GRCh38.p12 chr4\|NW_003315915.1: 269,739-326,294	LOC105378262
nsv4377883	copy number variation	50	nstd173	human		GRCh37 chr14: 41,610,544-41,657,457 , GRCh38.p12 chr14: 41,141,341-41,188,254	LINC02315
nsv4379737	copy number variation	349	nstd173	human		GRCh37 chr1: 169,216,099-169,241,765 , GRCh38.p12 chr1: 169,246,861-169,272,527	NME7
nsv4380931	copy number variation	2	nstd173	human		GRCh37 chrX: 8,180,047-8,271,157 , GRCh38.p12 chrX: 8,212,006-8,303,116	LOC107985675
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
nsv4385455	copy number variation	190	nstd173	human		GRCh37 chr20: 1,557,177-1,597,997 , GRCh38.p12 chr20: 1,576,531-1,617,351	SIRPB1
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
nsv4382253	copy number variation	206	nstd173	human		GRCh37 chr12: 11,503,225-11,553,849 , GRCh38.p12 chr12: 11,350,291-11,400,915 , GRCh38.p12 chr12\|NT_187658.1: 545,254-572,349	PRB2, PRB1
nsv4374620	copy number variation	41	nstd173	human		GRCh37 chr6: 257,340-381,137 , GRCh38.p12 chr6: 257,340-381,137	, DUSP22, 1 more genes
nsv4377852	copy number variation	4	nstd173	human		GRCh37 chr12: 7,976,421-8,124,048 , GRCh38.p12 chr12: 7,823,825-7,971,452	SLC2A3, LOC100130582, 3 more genes
nsv4381505	copy number variation	106	nstd173	human		GRCh37 chr11: 55,363,327-55,442,305 , GRCh38.p12 chr11: 55,595,851-55,674,829	OR4C11, OR4C6, 3 more genes
nsv4377785	copy number variation	2	nstd173	human		GRCh37 chr1: 1,352,534-1,443,716 , GRCh38.p12 chr1: 1,417,154-1,508,336	VWA1, ATAD3B, 6 more genes
nsv4369720	copy number variation	3	nstd173	human		GRCh37 chr16: 32,538,293-33,814,547 , GRCh38.p12 chr16: 32,526,972-34,012,080	IGHV3OR16-6, FAM153DP, 45 more genes
nsv4378128	copy number variation	463	nstd173	human		GRCh37 chr11: 51,337,076-51,376,963 , GRCh38.p12 chr11: 54,742,317-54,782,204	0
nsv4369967	copy number variation	1	nstd173	human		GRCh37 chr15: 100,987,919-101,615,876 , GRCh38.p12 chr15: 100,447,714-101,075,671	LOC105371026, LOC102723335, 14 more genes
nsv4385415	copy number variation	63	nstd173	human		GRCh37 chr17: 44,212,824-44,784,639 , GRCh38.p12 chr17: 46,135,458-46,707,273 , GRCh38.p12 chr17\|NT_187663.1: 837,565-1,226,699	DND1P2, RN7SL656P, 14 more genes
nsv4382725	copy number variation	1	nstd173	human		GRCh37 chr14: 22,476,432-22,959,555 , GRCh38.p12 chr14: 22,008,193-22,490,567	LOC100420343, TRAV26-1, 56 more genes
nsv4370415	copy number variation	102	nstd173	human		GRCh37 chr7: 38,294,983-38,394,857 , GRCh38.p12 chr7: 38,255,382-38,355,256	TRGV5, TRGV7, 19 more genes

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