1-0389-001 AND nstd173 - dbVar - NCBI

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Items: 15

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Number of Variants: 15

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4377189	copy number variation	2	nstd173	human		GRCh37 chr2: 98,118,115-98,166,865 , GRCh38.p12 chr2: 97,501,652-97,550,402	ANKRD36B
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
nsv4371805	copy number variation	282	nstd173	human		GRCh37 chr11: 18,941,197-18,961,975 , GRCh38.p12 chr11: 18,919,650-18,940,428	MRGPRX1
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
nsv4367142	copy number variation	135	nstd173	human		GRCh37 chr12: 2,235,941-2,259,954 , GRCh38.p12 chr12: 2,126,775-2,150,788 , GRCh38.p12 chr12\|NW_018654718.1: 468,919-492,932	LOC107984131, CACNA1C
nsv4383338	copy number variation	86	nstd173	human		GRCh37 chr1: 72,756,100-72,812,440 , GRCh38.p12 chr1: 72,290,417-72,346,757 , GRCh38.p12 chr1\|NW_018654707.1: 2,684-67,982	RPL31P12, LOC105378797
nsv4382503	copy number variation	75	nstd173	human		GRCh37 chr4: 69,367,105-69,485,978 , GRCh38.p12 chr4: 68,501,387-68,620,260	UGT2B29P, LOC100422402, 2 more genes
nsv4365887	copy number variation	2	nstd173	human		GRCh37 chr1: 1,621,786-1,675,061 , GRCh38.p12 chr1: 1,690,347-1,743,622	LOC100129381, MMP23A, 3 more genes
nsv4375662	copy number variation	272	nstd173	human		GRCh37 chr11: 5,783,910-5,809,230 , GRCh38.p12 chr11: 5,762,680-5,788,000	OR52N1, OR56B2P, 1 more genes
nsv4379698	copy number variation	3	nstd173	human		GRCh37 chr15: 82,439,438-82,622,366 , GRCh38.p12 chr15: 82,147,097-82,330,010	ADAMTS7P1, SAXO2, 2 more genes
nsv4382865	copy number variation	1	nstd173	human		GRCh37 chr1: 178,446,054-178,499,350 , GRCh38.p12 chr1: 178,476,919-178,530,215	RASAL2, TEX35, 3 more genes
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
nsv4381956	copy number variation	239	nstd173	human		GRCh37 chr5: 57,326,026-57,351,813 , GRCh38.p12 chr5: 58,030,199-58,055,986	0
nsv4377396	copy number variation	94	nstd173	human		GRCh37 chr14: 106,536,991-106,560,975 , GRCh38.p12 chr: NaN-NaN	0
nsv4379738	copy number variation	2	nstd173	human		GRCh37 chrX: 115,125,671-115,156,164 , GRCh38.p12 chrX: 116,009,338-116,024,911	0

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