OSC0308 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
nsv6628654	copy number variation	115	nstd224	human		GRCh37 chr3: 151,514,590-151,545,958 , GRCh38.p12 chr3: 151,796,802-151,828,170	AADAC, AADACL2-AS1
nsv6633357	copy number variation	8	nstd224	human		GRCh37 chr8: 87,201,127-87,330,713 , GRCh38.p12 chr8: 86,188,898-86,318,484	LOC105375623, SLC7A13
nsv6620897	copy number variation	2	nstd224	human		GRCh37 chr11: 134,367,820-134,738,885 , GRCh38.p12 chr11: 134,497,926-134,868,991	LINC02706, LOC105369583, 2 more genes
nsv6629304	copy number variation	2	nstd224	human		GRCh37 chr3: 75,407,145-75,554,281 , GRCh38.p12 chr3: 75,357,994-75,505,130	OR7E22P, ALG1L6P, 5 more genes
nsv6625746	copy number variation	93	nstd224	human		GRCh37 chr1: 12,852,872-12,921,278 , GRCh38.p12 chr1: 12,792,723-12,861,423 , GRCh38.p12 chr1\|NW_012132914.1: 1-42,936	PRAMEF1, PRAMEF2, 4 more genes
nsv6632435	copy number variation	1	nstd224	human		GRCh37 chr7: 72,083,747-72,413,618 , GRCh38.p12 chr7: 72,618,762-72,943,079	POM121, SBDSP1, 6 more genes
nsv6623373	copy number variation	1	nstd224	human		GRCh37 chr16: 15,126,744-15,381,715 , GRCh38.p12 chr16: 15,032,887-15,287,858 , GRCh38.p12 chr16\|NT_187607.1: 374,708-636,802	PDXDC1, MIR6511B2, 10 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
nsv6622971	copy number variation	23	nstd224	human		GRCh37 chr15: 22,382,854-22,503,228 , GRCh38.p12 chr15: 22,094,903-22,215,277	IGHV1OR15-1, LOC642131, 8 more genes

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