OSC7728 AND nstd224 - dbVar - NCBI

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Number of Variants: 11

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6629898	copy number variation	832	nstd224	human		GRCh37 chr4: 69,401,172-69,435,811 , GRCh38.p12 chr4: 68,535,454-68,570,093	UGT2B17
nsv6623129	copy number variation	1	nstd224	human		GRCh37 chr15: 59,281,369-59,313,825 , GRCh38.p12 chr15: 58,989,170-59,021,626	RNF111
nsv6625538	copy number variation	421	nstd224	human		GRCh37 chr1: 110,228,436-110,241,385 , GRCh38.p12 chr1: 109,685,814-109,698,763	GSTM1
nsv6632579	copy number variation	1	nstd224	human		GRCh37 chr8: 15,445,418-15,565,126 , GRCh38.p12 chr8: 15,587,909-15,707,617	TUSC3, LOC100431174
nsv6623651	copy number variation	160	nstd224	human		GRCh37 chr16: 32,509,483-32,650,542 , GRCh38.p12 chr16: 32,498,162-32,639,221	FAM153DP, LOC107984013
nsv6629567	copy number variation	1	nstd224	human		GRCh37 chr4: 159,588,973-159,616,703 , GRCh38.p12 chr4: 158,667,821-158,695,551	ETFDH, C4orf46
nsv6629247	copy number variation	65	nstd224	human		GRCh37 chr3: 75,447,252-75,550,939 , GRCh38.p12 chr3: 75,398,101-75,501,788	FAM86DP, LINC02018, 2 more genes
nsv6626928	copy number variation	93	nstd224	human		GRCh37 chr22: 24,374,253-24,386,612 , GRCh38.p12 chr22\|NT_187633.1: 268,428-280,787	GSTT1-AS1, GSTTP2, 2 more genes
nsv6624080	copy number variation	1	nstd224	human		GRCh37 chr17: 3,881,130-4,093,430 , GRCh38.p12 chr17: 3,977,836-4,190,135	ZZEF1, ANKFY1, 3 more genes
nsv6625471	copy number variation	6	nstd224	human		GRCh37 chr1: 104,084,742-104,153,766 , GRCh38.p12 chr1: 103,542,120-103,611,144	AMY2B, RNPC3, 1 more genes
nsv6622001	copy number variation	1	nstd224	human		GRCh37 chr14: 20,198,662-20,399,796 , GRCh38.p12 chr14: 19,730,503-19,931,637	OR4N1P, OR4K1, 11 more genes

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OSC7728 AND nstd224 (12)
dbVar

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