241423 AND nstd173 - dbVar - NCBI

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Items: 17

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Number of Variants: 17

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4366770	copy number variation	47	nstd173	human		GRCh37 chr16: 55,796,562-55,822,431 , GRCh38.p12 chr16: 55,762,650-55,788,519	CES1P1
nsv4372717	copy number variation	7	nstd173	human		GRCh37 chr1: 72,771,354-72,811,147 , GRCh38.p12 chr1: 72,305,671-72,345,464 , GRCh38.p12 chr1\|NW_018654707.1: 17,938-66,689	LOC105378797
nsv4367050	copy number variation	2	nstd173	human		GRCh37 chr12: 31,356,049-31,394,190 , GRCh38.p12 chr12: 31,203,115-31,241,256 , GRCh38.p12 chr12\|NT_187587.1: 93,909-132,050	LOC107987168
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
nsv4381558	copy number variation	4	nstd173	human		GRCh37 chr4: 38,463,618-38,542,496 , GRCh38.p12 chr4: 38,461,997-38,540,875	LINC01258, LINC01259
nsv4380060	copy number variation	2	nstd173	human		GRCh37 chr3: 186,386,546-186,422,122 , GRCh38.p12 chr3: 186,668,757-186,704,333	HRG, HRG-AS1, 1 more genes
nsv4386886	copy number variation	138	nstd173	human		GRCh37 chr19: 54,730,238-54,752,217 , GRCh38.p12 chr19: 54,226,365-54,248,358 , GRCh38.p12 chr19\|NT_187693.1: 201,352-223,331 , GRCh38.p12 chr19\|NW_003571060.1: 201,350-223,326 , GRCh38.p12 chr19\|NW_003571054.1: 201,165-223,093	LILRB5, LOC100421130, 3 more genes
nsv4367460	copy number variation	3	nstd173	human		GRCh37 chrX: 128,099,577-128,607,870 , GRCh38.p12 chrX: 128,965,600-129,473,893	RNA5SP513, SMARCA1, 3 more genes
nsv4368241	copy number variation	217	nstd173	human		GRCh37 chr17: 34,437,482-34,477,480 , GRCh38.p12 chr17: 36,110,089-36,150,098 , GRCh38.p12 chr17\|NT_187661.1: 64,186-104,195 , GRCh38.p12 chr17\|NT_187614.1: 345,010-385,008	LOC100419980, LOC101927369, 3 more genes
nsv4385606	copy number variation	9	nstd173	human		GRCh37 chr6: 257,340-294,431 , GRCh38.p12 chr6: 257,340-294,431	, DUSP22, 1 more genes
nsv4383402	copy number variation	3	nstd173	human		GRCh37 chr5: 120,683,328-120,709,623 , GRCh38.p12 chr5: 121,347,633-121,373,928	0
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
nsv4379292	copy number variation	3	nstd173	human		GRCh37 chr7: 70,558,485-70,580,268 , GRCh38.p12 chr7: 71,093,499-71,115,282	0
nsv4367603	copy number variation	1	nstd173	human		GRCh37 chrX: 37,227,417-37,532,841 , GRCh38.p12 chrX: 37,368,164-37,673,588	FAM47DP, LANCL3, 4 more genes
nsv4375396	copy number variation	1	nstd173	human		GRCh37 chr8: 25,820,075-27,117,359 , GRCh38.p12 chr8: 25,962,559-27,259,842	RPLP1P9, LOC105379336, 20 more genes
nsv4371527	copy number variation	186	nstd173	human		GRCh37 chr16: 34,449,595-34,755,828 , GRCh38.p12 chr16: 35,215,224-35,521,457	AGGF1P6, RARRES2P9, 27 more genes
nsv4383983	copy number variation	8	nstd173	human		GRCh37 chrX: 115,133,389-115,156,165 , GRCh38.p12 chr: NaN-NaN	0

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