IS33890 AND nstd71 - dbVar - NCBI

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Number of Variants: 16

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv895448	copy number variation	1	nstd71	human		NCBI36 chr10: 56,126,582-56,196,753 , GRCh37.p13 chr10: 56,456,576-56,526,747 , GRCh38.p12 chr10: 54,696,816-54,766,987	PCDH15
nsv890754	copy number variation	920	nstd71	human		NCBI36 chr8: 39,350,791-39,509,376 , GRCh37.p13 chr8: 39,231,634-39,390,219 , GRCh38.p12 chr8: 39,374,115-39,532,700	ADAM5, ADAM3A
nsv895564	copy number variation	1	nstd71	human		NCBI36 chr10: 60,890,929-60,997,508 , GRCh37.p13 chr10: 61,220,923-61,327,502 , GRCh38.p12 chr10: 59,461,165-59,567,744	MRPL50P4, LOC107984235
nsv907467	copy number variation	1	nstd71	human		NCBI36 chr17: 759,500-770,573 , GRCh37.p13 chr17: 812,750-823,823 , GRCh38.p12 chr17: 909,510-920,583	NXN, LOC101927727
nsv872992	copy number variation	87	nstd71	human		NCBI36 chr1: 194,977,690-195,089,653 , GRCh37.p13 chr1: 196,711,067-196,823,030 , GRCh38.p12 chr1: 196,741,937-196,853,900	LOC100996886, CFHR3, 2 more genes
nsv871196	copy number variation	88	nstd71	human		NCBI36 chr1: 12,777,429-12,810,136 , GRCh37.p13 chr1: 12,854,842-12,887,549 , GRCh38.p12 chr1: 12,794,693-12,827,690	PRAMEF11, PRAMEF1, 1 more genes
nsv878206	copy number variation	2	nstd71	human		NCBI36 chr3: 198,987,300-199,079,364 , GRCh37.p13 chr3: 197,502,903-197,594,967 , GRCh38.p12 chr3: 197,776,032-197,868,096	LOC105374310, FYTTD1, 2 more genes
nsv879332	copy number variation	32	nstd71	human		NCBI36 chr4: 69,097,539-69,179,871 , GRCh37.p13 chr4: 69,414,944-69,497,276 , GRCh38.p12 chr4: 68,549,226-68,631,558	LOC100132651, LOC728807, 2 more genes
nsv872544	copy number variation	1	nstd71	human		NCBI36 chr1: 169,883,445-169,921,591 , GRCh37.p13 chr1: 171,616,822-171,654,968 , GRCh38.p12 chr1: 171,647,682-171,685,828	PFN1P1, RPL4P3, 1 more genes
nsv879365	copy number variation	34	nstd71	human		NCBI36 chr4: 69,163,188-69,405,358 , GRCh37.p13 chr: NaN-NaN , GRCh38.p12 chr: NaN-NaN	0
nsv874027	copy number variation	19	nstd71	human		NCBI36 chr2: 49,715,638-49,809,930 , GRCh37.p13 chr2: 49,862,134-49,956,426 , GRCh38.p12 chr2: 49,634,996-49,729,288	0
nsv886057	copy number variation	200	nstd71	human		NCBI36 chr6: 67,065,007-67,111,682 , GRCh37.p13 chr6: 67,008,286-67,054,961 , GRCh38.p12 chr6: 66,298,393-66,345,068	0
nsv876893	copy number variation	298	nstd71	human		NCBI36 chr3: 65,159,939-65,190,844 , GRCh37.p13 chr3: 65,184,899-65,215,804 , GRCh38.p12 chr3: 65,199,224-65,230,129	0
nsv902407	copy number variation	1	nstd71	human		NCBI36 chr14: 104,225,150-104,339,273 , GRCh37.p13 chr14: 105,154,105-105,268,228 , GRCh38.p12 chr14: 104,687,768-104,801,891	AKT1, INF2, 6 more genes
nsv913202	copy number variation	2	nstd71	human		NCBI36 chr20: 61,562,786-61,673,128 , GRCh37.p13 chr20: 62,092,342-62,202,684 , GRCh38.p12 chr20: 63,460,989-63,571,331	HELZ2, KCNQ2, 7 more genes
nsv902520	copy number variation	31	nstd71	human		NCBI36 chr14: 105,083,528-105,259,090 , GRCh37.p13 chr14: 106,012,483-106,188,045 , GRCh37.p13 chr14\|NW_004166863.1: 209,313-384,875 , GRCh38.p12 chr14\|NT_187600.1: 13,144-189,477 , GRCh38.p12 chr14: 105,546,146-105,721,708	MIR8071-2, IGH, 15 more genes

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