OSC4792 AND nstd224 - dbVar - NCBI

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Items: 11

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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
nsv6621510	copy number variation	1	nstd224	human		GRCh37 chr12: 124,284,762-124,303,745 , GRCh38.p12 chr12: 123,800,215-123,819,198	DNAH10
nsv6625677	copy number variation	3	nstd224	human		GRCh37 chr1: 17,216,331-17,250,945 , GRCh38.p12 chr1: 16,889,836-16,924,450	TRN-GTT4-1, CROCC, 3 more genes
nsv6627056	copy number variation	6	nstd224	human		GRCh37 chr22: 18,892,575-19,016,663 , GRCh38.p12 chr22: 18,905,062-19,029,150	PRODH, DGCR6, 1 more genes
nsv6628083	copy number variation	1	nstd224	human		GRCh37 chr2: 241,626,057-241,699,883 , GRCh38.p12 chr2: 240,686,640-240,760,466	LOC285191, KIF1A, 1 more genes
nsv6622894	copy number variation	1	nstd224	human		GRCh37 chr15: 43,892,807-43,925,022 , GRCh38.p12 chr15: 43,600,609-43,632,824	CATSPER2, RNU6-554P, 2 more genes
nsv6625000	copy number variation	1	nstd224	human		GRCh37 chr19: 43,513,659-43,698,669 , GRCh38.p12 chr19: 43,009,507-43,194,517	CEACAMP8, CEACAMP9, 5 more genes
nsv6621567	copy number variation	64	nstd224	human		GRCh37 chr12: 131,730,317-131,824,796 , GRCh38.p12 chr12: 131,245,772-131,340,251	LOC100128002, RPS6P20, 4 more genes
nsv6628864	copy number variation	24	nstd224	human		GRCh37 chr3: 65,193,246-65,221,937 , GRCh38.p12 chr3: 65,207,571-65,236,262	0
nsv6632275	copy number variation	68	nstd224	human		GRCh37 chr7: 8,838,717-8,855,423 , GRCh38.p12 chr7: 8,799,087-8,815,793	0
nsv6625827	copy number variation	1	nstd224	human		GRCh38.p12 chr: NaN-NaN , GRCh37 chr1: 144,816,621-145,281,993	0
nsv6622241	copy number variation	2	nstd224	human		GRCh37 chr14: 20,216,352-20,416,499 , GRCh38.p12 chr14: 19,748,193-19,948,340	OR4K4P, OR4H12P, 10 more genes

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OSC4792 AND nstd224 (12)
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