2-1618-003 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
nsv4387213	copy number variation	434	nstd173	human		GRCh37 chr4: 34,779,032-34,824,730 , GRCh38.p12 chr4: 34,777,410-34,823,108 , GRCh38.p12 chr4\|NW_003315915.1: 269,739-315,437	LOC105378262
nsv4388221	copy number variation	6	nstd173	human		GRCh37 chr3: 84,844,800-84,873,060 , GRCh38.p12 chr3: 84,795,649-84,823,909 , GRCh38.p12 chr3\|NW_018654711.1: 1-23,942	LINC00971
nsv4388190	copy number variation	1	nstd173	human		GRCh37 chrX: 8,173,021-8,271,157 , GRCh38.p12 chrX: 8,204,980-8,303,116	LOC107985675
nsv4378345	copy number variation	9	nstd173	human		GRCh37 chr4: 161,952,214-162,007,295 , GRCh38.p12 chr4: 161,031,062-161,086,143	LOC105377514
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
nsv4386789	copy number variation	5	nstd173	human		GRCh37 chr12: 11,503,087-11,553,849 , GRCh38.p12 chr12: 11,350,153-11,400,915 , GRCh38.p12 chr12\|NT_187658.1: 545,116-572,349	PRB1, PRB2
nsv4386964	copy number variation	5	nstd173	human		GRCh37 chr1: 1,402,894-1,429,151 , GRCh38.p12 chr1: 1,467,514-1,493,771	ATAD3C, ATAD3B
nsv4370464	copy number variation	362	nstd173	human		GRCh37 chr11: 4,967,239-4,991,060 , GRCh38.p12 chr11: 4,946,009-4,969,830	OR51A4, OR51A2
nsv4383147	copy number variation	2	nstd173	human		GRCh37 chr3: 295,781-354,495 , GRCh38.p12 chr3: 254,098-312,812	RPS8P6, CHL1, 1 more genes
nsv4375232	copy number variation	423	nstd173	human		GRCh37 chr5: 180,375,302-180,430,801 , GRCh38.p12 chr5: 180,948,302-181,003,801	BTNL8, LOC100128762, 3 more genes
nsv4382082	copy number variation	609	nstd173	human		GRCh37 chr11: 55,374,019-55,442,305 , GRCh38.p12 chr11: 55,606,543-55,674,829	OR4C6, OR4P4, 2 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
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
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
nsv4382768	copy number variation	92	nstd173	human		GRCh37 chr4: 10,209,966-10,240,250 , GRCh38.p12 chr4: 10,208,342-10,238,626	0
nsv4380160	copy number variation	62	nstd173	human		GRCh37 chr6: 110,394,605-110,415,415 , GRCh38.p12 chr6: 110,073,402-110,094,212	0
nsv4376424	copy number variation	1	nstd173	human		GRCh37 chr15: 100,987,919-101,612,249 , GRCh38.p12 chr15: 100,447,714-101,072,044	LOC105371026, LOC102723335, 14 more genes
nsv4368355	copy number variation	2	nstd173	human		GRCh37 chr10: 20,790,184-20,811,442 , GRCh38.p12 chr10: 20,501,255-20,522,513	0

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