OSC6527 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
nsv6629381	copy number variation	8	nstd224	human		GRCh37 chr4: 168,818,443-168,991,763 , GRCh38.p12 chr4: 167,897,292-168,070,612	LOC105377523
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
nsv6627557	copy number variation	30	nstd224	human		GRCh37 chr2: 228,241,621-228,257,995 , GRCh38.p12 chr2: 227,376,905-227,393,279	TM4SF20
nsv6624960	copy number variation	42	nstd224	human		GRCh37 chr19: 41,355,925-41,387,391 , GRCh38.p12 chr19: 40,850,020-40,881,486	CYP2A7, CYP2A6
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
nsv6623217	copy number variation	1	nstd224	human		GRCh37 chr16: 33,546,028-33,602,834 , GRCh38.p12 chr16: 33,743,561-33,800,367	LOC102724207, ENPP7P13
nsv6621456	copy number variation	4	nstd224	human		GRCh37 chr12: 31,266,287-31,383,052 , GRCh38.p12 chr12: 31,113,353-31,230,118 , GRCh38.p12 chr12\|NT_187587.1: 1,874-120,912	OVOS2, LOC101060058, 1 more genes
nsv6627380	copy number variation	480	nstd224	human		GRCh37 chr22: 24,374,253-24,390,432 , GRCh38.p12 chr22\|NT_187633.1: 268,428-284,607	GSTTP2, GSTT1-AS1, 2 more genes
nsv6633430	copy number variation	152	nstd224	human		GRCh37 chr9: 24,505,147-24,518,795 , GRCh38.p12 chr9: 24,505,149-24,518,797	0
nsv6623220	copy number variation	151	nstd224	human		GRCh37 chr16: 34,489,371-34,724,788 , GRCh38.p12 chr16: 35,255,000-35,490,417	AGGF1P4, C2orf69P3, 21 more genes

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OSC6527 AND nstd224 (11)
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