M2251 AND nstd157 - dbVar - NCBI

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Number of Variants: 12

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3317544	copy number variation	2	nstd157	human		GRCh37 chr11: 83,829,316-83,843,764 , GRCh38.p12 chr11: 84,118,273-84,132,721	DLG2
nsv3318023	copy number variation	1	nstd157	human		GRCh38.p12 chr16: 5,581,724-5,630,103 , GRCh37 chr16: 5,631,725-5,680,104	RBFOX1, LINC01570
nsv3318791	copy number variation	1	nstd157	human		GRCh38.p12 chr1: 19,676,025-19,706,642 , GRCh37 chr1: 20,002,518-20,033,135	HTR6, TMCO4
nsv3318588	copy number variation	20	nstd157	human		GRCh38.p12 chr2: 38,729,805-38,744,481 , GRCh37 chr2: 38,956,947-38,971,623	SRSF7, GALM
nsv3318457	copy number variation	10	nstd157	human		GRCh38.p12 chr6: 266,035-379,638 , GRCh37 chr6: 266,035-379,638	DUSP22, , 1 more genes
nsv3317105	copy number variation	1	nstd157	human		GRCh38.p12 chr4: 134,941,607-134,979,388 , GRCh37 chr4: 135,862,762-135,900,543	RPS2P27, LOC105377437, 1 more genes
nsv3318316	copy number variation	72	nstd157	human		GRCh37 chr14: 41,615,868-41,661,685 , GRCh38.p12 chr14: 41,146,665-41,192,482	0
nsv3317783	copy number variation	1	nstd157	human		GRCh37 chr3: 134,339,879-134,707,498 , GRCh38.p12 chr3: 134,621,037-134,988,656	EPHB1, CEP63, 4 more genes
nsv3318081	copy number variation	3	nstd157	human		GRCh38.p12 chr4: 11,871,409-11,878,537 , GRCh37 chr4: 11,873,033-11,880,161	0
nsv3318585	copy number variation	18	nstd157	human		GRCh38.p12 chr4: 59,459,292-59,465,162 , GRCh37 chr4: 60,325,010-60,330,880	0
nsv3318370	copy number variation	14	nstd157	human		GRCh37 chr18: 63,200,484-63,206,335 , GRCh38.p12 chr18: 65,533,248-65,539,099	0
nsv3317174	copy number variation	1	nstd157	human		GRCh38.p12 chr4: 137,887,487-137,892,523 , GRCh37 chr4: 138,808,641-138,813,677	0

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