OSC7733 AND nstd224 - dbVar - NCBI

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Items: 9

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Number of Variants: 9

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6625091	copy number variation	291	nstd224	human		GRCh37 chr1: 110,228,505-110,241,385 , GRCh38.p12 chr1: 109,685,883-109,698,763	GSTM1
nsv6633630	copy number variation	1	nstd224	human		GRCh37 chr9: 21,056,582-21,080,518 , GRCh38.p12 chr9: 21,056,583-21,080,519	IFNB1, IFNNP1
nsv6626097	copy number variation	1	nstd224	human		GRCh37 chr1: 223,799,540-223,857,750 , GRCh38.p12 chr1: 223,611,838-223,670,048	SNRPEP10, CAPN8
nsv6624685	copy number variation	256	nstd224	human		GRCh37 chr19: 20,605,360-20,700,135 , GRCh38.p12 chr19: 20,422,554-20,517,329	BNIP3P23, LOC105372317, 2 more genes
nsv6623069	copy number variation	1	nstd224	human		GRCh37 chr15: 30,940,504-31,092,983 , GRCh38.p12 chr15: 30,648,301-30,800,780 , GRCh38.p12 chr15\|NT_187660.1: 2,933,835-3,086,491 , GRCh38.p12 chr15\|NW_011332701.1: 2,821,383-2,974,039	ARHGAP11B, LOC100288637, 2 more genes
nsv6630498	copy number variation	1	nstd224	human		GRCh37 chr5: 175,556,343-175,606,174 , GRCh38.p12 chr5: 176,129,340-176,179,171	CEP192P1, SEPHS1P3, 1 more genes
nsv6627470	copy number variation	16	nstd224	human		GRCh37 chr22: 42,523,678-42,536,064 , GRCh38.p12 chr22\|NT_187682.1: 50,017-62,403	CYP2D6, CYP2D7, 1 more genes
nsv6624541	copy number variation	1	nstd224	human		GRCh37 chr18: 14,550,022-14,734,925 , GRCh38.p12 chr18: 14,550,023-14,734,926	OR4K7P, OR4K8P, 7 more genes
nsv6630250	copy number variation	1	nstd224	human		GRCh37 chr5: 101,478,928-101,522,676 , GRCh38.p12 chr5: 102,143,224-102,186,972	0

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