OSC4223 AND nstd224 - dbVar - NCBI

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Number of Variants: 10

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6632327	copy number variation	204	nstd224	human		GRCh37 chr8: 137,688,230-137,852,251 , GRCh38.p12 chr8: 136,675,987-136,840,008	LINC02055
nsv6632654	copy number variation	1	nstd224	human		GRCh37 chr8: 112,589,344-112,713,528 , GRCh38.p12 chr8: 111,577,115-111,701,299	H2AZP7
nsv6631842	copy number variation	101	nstd224	human		GRCh37 chr7: 142,829,211-142,881,461 , GRCh38.p12 chr7: 143,132,118-143,184,368	PIP, TAS2R39
nsv6633983	copy number variation	5	nstd224	human		GRCh37 chr9: 30,646,764-30,698,142 , GRCh38.p12 chr9: 30,646,766-30,698,144	RBMXP2, CDRT15P5
nsv6626735	copy number variation	4	nstd224	human		GRCh37 chr21: 10,906,922-11,098,723 , GRCh38.p12 chr21: 10,413,734-10,605,535	TPTE, BAGE2, 1 more genes
nsv6626817	copy number variation	29	nstd224	human		GRCh37 chr21: 14,669,931-14,844,368 , GRCh38.p12 chr21: 13,297,610-13,472,047	GTF2IP2, MIR3156-3, 2 more genes
nsv6625711	copy number variation	21	nstd224	human		GRCh37 chr1: 196,712,596-196,801,025 , GRCh38.p12 chr1: 196,743,466-196,831,895	CFH, CFHR1, 1 more genes
nsv6620485	copy number variation	471	nstd224	human		GRCh37 chr10: 47,543,322-47,703,946 , GRCh38.p12 chr10: 46,172,086-46,332,710	AHCYP1, ANTXRL, 2 more genes
nsv6621655	copy number variation	8	nstd224	human		GRCh37 chr13: 19,121,950-19,263,735 , GRCh38.p12 chr13: 18,547,810-18,689,595	TERF1P5, FEM1AP4, 1 more genes
nsv6620265	copy number variation	201	nstd224	human		GRCh37 chr10: 135,256,762-135,379,710 , GRCh38.p12 chr10: 133,443,258-133,566,206	CYP2E1, OR7M1P, 4 more genes

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OSC4223 AND nstd224 (11)
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