1-0886-003 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
nsv4368568	copy number variation	177	nstd173	human		GRCh37 chr14: 41,610,556-41,657,457 , GRCh38.p12 chr14: 41,141,353-41,188,254	LINC02315
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
nsv4376609	copy number variation	40	nstd173	human		GRCh37 chr7: 141,755,372-141,789,964 , GRCh38.p12 chr7: 142,055,572-142,090,164 , GRCh38.p12 chr7\|NT_187562.1: 17,452-52,044	MGAM
nsv4388578	copy number variation	7	nstd173	human		GRCh37 chr8: 89,689,592-89,713,184 , GRCh38.p12 chr8: 88,677,363-88,700,955	LOC105375630
nsv4385871	copy number variation	3	nstd173	human		GRCh37 chr14: 86,460,915-86,500,283 , GRCh38.p12 chr14: 85,994,571-86,033,939	LINC02328, LINC02316
nsv4381433	copy number variation	68	nstd173	human		GRCh37 chr1: 196,827,842-196,877,049 , GRCh38.p12 chr1: 196,858,712-196,907,919	LOC100996886, CFHR4
nsv4380961	copy number variation	18	nstd173	human		GRCh37 chr21: 20,057,678-20,078,424 , GRCh38.p12 chr21: 18,685,360-18,706,106	MIR548X, MIR548XHG
nsv4383067	copy number variation	10	nstd173	human		GRCh37 chr11: 55,374,031-55,460,788 , GRCh38.p12 chr11: 55,606,555-55,693,312	OR4P1P, OR4P4, 3 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
nsv4370259	copy number variation	2	nstd173	human		GRCh37 chr6: 257,049-294,286 , GRCh38.p12 chr6: 257,049-294,286	, DUSP22, 1 more genes
nsv4368821	copy number variation	1373	nstd173	human		GRCh37 chr22: 24,353,749-24,385,040 , GRCh38.p12 chr22\|NT_187633.1: 247,924-279,215	LOC391322, GSTTP2, 3 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
nsv4387125	copy number variation	432	nstd173	human		GRCh37 chr2: 35,967,123-35,997,473 , GRCh38.p12 chr2: 35,742,057-35,772,407	0
nsv4386306	copy number variation	141	nstd173	human		GRCh37 chrX: 924,088-944,608 , GRCh38.p12 chrX: 963,353-983,873	0
nsv4384501	copy number variation	242	nstd173	human		GRCh37 chr16: 19,945,795-19,965,942 , GRCh38.p12 chr16: 19,934,473-19,954,620	0
nsv4374799	copy number variation	11	nstd173	human		GRCh37 chr10: 46,966,534-47,688,677 , GRCh38.p12 chr10: 46,157,935-47,923,579	FAM25BP, RN7SL248P, 54 more genes
nsv4368684	copy number variation	2	nstd173	human		GRCh37 chr14: 22,533,211-22,960,757 , GRCh38.p12 chr14: 22,064,947-22,491,770	TRAV24, TRAJ50, 54 more genes
nsv4384388	copy number variation	3	nstd173	human		GRCh37 chr10: 135,234,127-135,404,224 , GRCh38.p12 chr10: 133,420,623-133,590,720	LOC105378575, SPRN, 10 more genes
nsv4372987	copy number variation	10	nstd173	human		GRCh37 chr7: 38,294,088-38,405,084 , GRCh38.p12 chr7: 38,254,487-38,365,483	TRG-AS1, TRGV3, 21 more genes

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