M2157 AND nstd157 - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
nsv3318006	copy number variation	1	nstd157	human	GRCh37 chr11: 3,823,407-3,844,254 , GRCh38.p12 chr11: 3,802,177-3,823,024	PGAP2
nsv3318458	copy number variation	16	nstd157	human	GRCh37 chr8: 16,262,222-16,272,444 , GRCh38.p12 chr8: 16,404,713-16,414,935	LOC101929028
nsv3317666	copy number variation	21	nstd157	human	GRCh37 chr21: 10,715,343-10,883,039 , GRCh38.p12 chr21: 10,629,418-10,797,114	IGHV1OR21-1
nsv3318592	copy number variation	5	nstd157	human	GRCh37 chr3: 8,825,626-8,858,081 , GRCh38.p12 chr3: 8,783,940-8,816,395	LOC107986061
nsv3317308	copy number variation	3	nstd157	human	GRCh37 chr5: 5,684,266-5,713,766 , GRCh38.p12 chr5: 5,684,153-5,713,653	LOC105374634
nsv3317692	copy number variation	1	nstd157	human	GRCh38.p12 chr12: 7,884,275-7,915,631 , GRCh37 chr12: 8,036,871-8,068,227	SLC2A14, NANOGP1
nsv3317223	copy number variation	4	nstd157	human	GRCh38.p12 chr16: 75,530,389-75,544,521 , GRCh37 chr16: 75,564,287-75,578,419	CHST5, TMEM231
nsv3317846	copy number variation	16	nstd157	human	GRCh38.p12 chr9: 133,071,778-133,082,065 , GRCh37 chr9: 135,947,165-135,957,452	CEL, CELP
nsv3318220	copy number variation	21	nstd157	human	GRCh38.p12 chr19: 20,418,529-20,532,427 , GRCh37 chr19: 20,601,335-20,715,233	ZNF826P, ZNF737, 3 more genes
nsv3317392	copy number variation	23	nstd157	human	GRCh38.p12 chr4: 68,527,638-68,623,755 , GRCh37 chr4: 69,393,356-69,489,473	UGT2B17, LOC100132651, 1 more genes
nsv3318700	copy number variation	1	nstd157	human	GRCh38.p12 chr1: 16,294,937-16,371,142 , GRCh37 chr1: 16,621,432-16,697,637	SZRD1, FBXO42, 1 more genes
nsv3318575	copy number variation	1	nstd157	human	GRCh38.p12 chr12: 7,856,516-7,871,347 , GRCh37 chr12: 8,009,112-8,023,943	SLC2A14, LOC100130582, 1 more genes
nsv3317450	copy number variation	4	nstd157	human	GRCh37 chr7: 102,017,833-102,339,500 , GRCh38.p12 chr7: 102,377,386-102,699,053	POLR2J, RASA4, 18 more genes
nsv3318549	copy number variation	16	nstd157	human	GRCh38.p12 chr: NaN-NaN , GRCh37 chr20: 29,652,403-29,842,291	0
nsv3318172	copy number variation	11	nstd157	human	GRCh37 chr14: 86,285,493-86,312,888 , GRCh38.p12 chr14: 85,819,149-85,846,544	0
nsv3317321	copy number variation	1	nstd157	human	GRCh37 chr4: 187,747,224-187,758,032 , GRCh38.p12 chr4: 186,826,070-186,836,878	0
nsv3318303	copy number variation	8	nstd157	human	GRCh37 chr8: 15,778,007-15,786,889 , GRCh38.p12 chr8: 15,920,498-15,929,380	0
nsv3318230	copy number variation	25	nstd157	human	GRCh37 chr2: 184,795,725-184,803,456 , GRCh38.p12 chr2: 183,930,998-183,938,729	0
nsv3318819	copy number variation	7	nstd157	human	GRCh37 chr5: 98,090,590-98,096,735 , GRCh38.p12 chr5: 98,754,886-98,761,031	0
nsv3317579	copy number variation	4	nstd157	human	GRCh37 chr1: 107,656,356-107,661,606 , GRCh38.p12 chr1: 107,113,734-107,118,984	0

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Number of Variants: 20

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