sample297 AND nstd145 - 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
nsv3116351	copy number variation	2	nstd145	human		GRCh37 chr16: 55,794,900-55,832,503 , GRCh38.p12 chr16: 55,760,988-55,798,591	CES1P1
nsv3113566	copy number variation	1	nstd145	human		GRCh37 chr16: 6,967,494-6,977,780 , GRCh38.p12 chr16: 6,917,493-6,927,779	RBFOX1
nsv3117364	copy number variation	1	nstd145	human		GRCh37 chr8: 2,150,517-2,158,871 , GRCh38.p12 chr8: 2,202,878-2,211,200 , GRCh38.p12 chr8\|NT_187576.1: 385,727-394,081	LOC105377782
nsv3117486	copy number variation	1	nstd145	human		GRCh37 chr7: 110,182,897-110,188,820 , GRCh38.p12 chr7: 110,542,840-110,548,763	LOC105375451
nsv3116148	copy number variation	97	nstd145	human		GRCh37 chr8: 594,429-599,002 , GRCh38.p12 chr8: 644,429-649,002	ERICH1
nsv3110593	copy number variation	88	nstd145	human		GRCh37 chr8: 40,774,871-40,779,295 , GRCh38.p12 chr8: 40,917,352-40,921,776	LOC105379389
nsv3114868	copy number variation	1	nstd145	human		GRCh37 chr6: 101,934,608-101,938,241 , GRCh38.p12 chr6: 101,486,732-101,490,365	GRIK2
nsv3113111	copy number variation	1	nstd145	human		GRCh37 chr5: 32,125,197-32,156,794 , GRCh38.p12 chr5: 32,125,091-32,156,688	GOLPH3
nsv3117756	copy number variation	6	nstd145	human		GRCh37 chr1: 248,739,582-248,795,189 , GRCh38.p12 chr1: 248,576,281-248,631,888	OR2T10, OR2T11
nsv3113959	copy number variation	1	nstd145	human		GRCh37 chr2: 109,932,195-109,934,252 , GRCh38.p12 chr2: 109,315,739-109,317,796	SH3RF3
nsv3110765	copy number variation	1	nstd145	human		GRCh37 chr6: 32,594,289-32,627,343 , GRCh38.p12 chr6: 32,626,512-32,659,566	HLA-DQA1, HLA-DQB1, 2 more genes
nsv3118226	copy number variation	38	nstd145	human		GRCh37 chr6: 103,737,412-103,760,261 , GRCh38.p12 chr6: 103,289,537-103,312,386	0
nsv3112313	copy number variation	7	nstd145	human		GRCh37 chr14: 40,610,218-40,616,291 , GRCh38.p12 chr14: 40,141,014-40,147,087	0
nsv3118092	copy number variation	1	nstd145	human		GRCh37 chr12: 33,386,861-33,392,588 , GRCh38.p12 chr12: 33,233,926-33,239,653	0
nsv3113061	copy number variation	4	nstd145	human		GRCh37 chr11: 37,614,635-37,617,557 , GRCh38.p12 chr11: 37,593,085-37,596,007	0

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