OSC2449 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
nsv6620321	copy number variation	1	nstd224	human		GRCh37 chr10: 12,923,638-12,945,749 , GRCh38.p12 chr10: 12,881,638-12,903,749	CCDC3
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
nsv6634038	copy number variation	5	nstd224	human		GRCh37 chrX: 103,259,022-103,295,458 , GRCh38.p12 chrX: 104,004,450-104,040,891	H2BW2, H2BW1
nsv6625095	copy number variation	4	nstd224	human		GRCh37 chr1: 110,230,836-110,253,241 , GRCh38.p12 chr1: 109,688,214-109,710,619	GSTM5, GSTM1
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
nsv6621388	copy number variation	34	nstd224	human		GRCh37 chr12: 8,003,758-8,101,326 , GRCh38.p12 chr12: 7,851,162-7,948,730	SLC2A3, NANOGP1, 3 more genes
nsv6620147	copy number variation	3	nstd224	human		GRCh37 chr10: 46,968,668-47,000,252 , GRCh38.p12 chr10: 46,549,365-46,580,949	SYT15, SYT15-AS1, 1 more genes
nsv6634258	copy number variation	1	nstd224	human		GRCh37 chrX: 48,074,408-48,163,105 , GRCh38.p12 chrX: 48,214,973-48,303,670	SSX1, SSX9P, 6 more genes
nsv6629065	copy number variation	500	nstd224	human		GRCh37 chr3: 65,193,246-65,211,507 , GRCh38.p12 chr3: 65,207,571-65,225,832	0
nsv6625059	copy number variation	14	nstd224	human		GRCh37 chr19: 6,896,471-7,103,542 , GRCh38.p12 chr19: 6,896,460-7,103,531	ZNF557, MBD3L5, 9 more genes
nsv6623615	copy number variation	320	nstd224	human		GRCh37 chr16: 34,516,075-34,686,820 , GRCh38.p12 chr16: 35,281,704-35,452,449	AGGF1P4, FRG2IP, 14 more genes

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OSC2449 AND nstd224 (12)
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