14-0258-003 AND nstd173 - dbVar - NCBI

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Items: 14

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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
nsv4385917	copy number variation	155	nstd173	human		GRCh37 chr2: 98,138,417-98,162,188 , GRCh38.p12 chr2: 97,521,954-97,545,725	ANKRD36B
nsv4378600	copy number variation	15	nstd173	human		GRCh37 chr6: 124,435,274-124,470,365 , GRCh38.p12 chr6: 124,114,129-124,149,220	NKAIN2
nsv4375285	copy number variation	1	nstd173	human		GRCh37 chr12: 85,906,037-86,045,154 , GRCh38.p12 chr12: 85,512,259-85,651,376	LOC101059974, LINC02820
nsv4375646	copy number variation	78	nstd173	human		GRCh37 chr1: 72,762,663-72,810,925 , GRCh38.p12 chr1: 72,296,980-72,345,242 , GRCh38.p12 chr1\|NW_018654707.1: 9,247-66,467	LOC105378797, RPL31P12
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
nsv4384457	copy number variation	635	nstd173	human		GRCh37 chr11: 55,374,031-55,453,008 , GRCh38.p12 chr11: 55,606,555-55,685,532	OR4P1P, OR4C6, 3 more genes
nsv4375714	copy number variation	376	nstd173	human		GRCh37 chr4: 69,435,889-69,485,978 , GRCh38.p12 chr4: 68,570,171-68,620,260	UGT2B17, LOC100132651, 1 more genes
nsv4384913	copy number variation	12	nstd173	human		GRCh37 chr17: 34,440,089-34,477,480 , GRCh38.p12 chr17: 36,112,696-36,150,098 , GRCh38.p12 chr17\|NT_187661.1: 66,793-104,195 , GRCh38.p12 chr17\|NT_187614.1: 347,617-385,008	, LOC101927369, 2 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
nsv4376025	copy number variation	1	nstd173	human		GRCh37 chr12: 11,216,817-11,239,823 , GRCh38.p12 chr12: 11,064,218-11,087,224	PRH1-PRR4, TAS2R64P, 2 more genes
nsv4387956	copy number variation	9	nstd173	human		GRCh37 chr14: 106,560,963-106,777,343 , GRCh38.p12 chr14: 106,112,755-106,321,086	IGHV3-13, IGHV3-19, 30 more genes
nsv4368660	copy number variation	868	nstd173	human		GRCh37 chr6: 103,738,197-103,759,824 , GRCh38.p12 chr6: 103,290,322-103,311,949	0
nsv4386552	copy number variation	30	nstd173	human		GRCh37 chr11: 54,701,512-54,788,759 , GRCh38.p12 chr11: 54,934,036-55,021,283	0
nsv4387566	copy number variation	315	nstd173	human		GRCh37 chr2: 34,701,655-34,727,784 , GRCh38.p12 chr2: 34,476,588-34,502,717	0

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