16-1004-003 AND nstd173 - dbVar - NCBI

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Number of Variants: 14

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4385759	copy number variation	9	nstd173	human		GRCh37 chr1: 73,007,962-73,086,201 , GRCh38.p12 chr1: 72,542,279-72,620,518	LOC105378797
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
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
nsv4379812	copy number variation	1	nstd173	human		GRCh37 chr3: 89,394,638-89,419,375 , GRCh38.p12 chr3: 89,345,488-89,370,225	EPHA3
nsv4365093	copy number variation	508	nstd173	human		GRCh37 chr13: 57,758,269-57,778,379 , GRCh38.p12 chr13: 57,184,135-57,204,245	MTCO2P3
nsv4368434	copy number variation	189	nstd173	human		GRCh37 chr1: 72,771,366-72,812,440 , GRCh38.p12 chr1: 72,305,683-72,346,757 , GRCh38.p12 chr1\|NW_018654707.1: 17,950-67,982	LOC105378797
nsv4379497	copy number variation	1	nstd173	human		GRCh37 chrX: 134,754,594-134,802,940 , GRCh38.p12 chrX: 135,620,669-135,669,225	SAGE4P, SAGE3P
nsv4366841	copy number variation	35	nstd173	human		GRCh37 chr1: 104,109,088-104,132,197 , GRCh38.p12 chr1: 103,566,466-103,589,575	ACTG1P4, AMY2B
nsv4385330	copy number variation	98	nstd173	human		GRCh37 chr6: 257,340-294,826 , GRCh38.p12 chr6: 257,340-294,826	, , 1 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
nsv4387023	copy number variation	344	nstd173	human		GRCh37 chr2: 34,701,643-34,727,784 , GRCh38.p12 chr2: 34,476,576-34,502,717	0
nsv4369274	copy number variation	262	nstd173	human		GRCh37 chr2: 35,976,209-35,997,473 , GRCh38.p12 chr2: 35,751,143-35,772,407	0
nsv4379973	copy number variation	66	nstd173	human		GRCh37 chr5: 676,873-821,699 , GRCh38.p12 chr5: 676,758-821,584	ZDHHC11B, , 4 more genes
nsv4386009	copy number variation	97	nstd173	human		GRCh37 chr5: 57,326,026-57,349,986 , GRCh38.p12 chr5: 58,030,199-58,054,159	0

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16-1004-003 AND nstd173 (15)
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