CONTROL_94 AND nstd53 - dbVar - NCBI

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Items: 8

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Number of Variants: 8

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv870002	copy number variation	49	nstd53	human		NCBI36 chr17: 41,527,764-41,566,540 , GRCh37.p13 chr17: 44,176,718-44,210,763 , GRCh38.p12 chr17: 46,094,581-46,133,397 , GRCh38.p12 chr17\|NT_187663.1: 796,687-835,504 , GRCh37.p13 chr17\|NT_167251.1: 655,282-689,337 , GRCh38.p12 chr17\|NT_167251.2: 653,289-691,821	KANSL1
nsv870438	copy number variation	2	nstd53	human		GRCh37.p13 chr3: 118,732,054-118,824,020 , GRCh38.p12 chr3: 119,013,207-119,105,173 , NCBI36 chr3: 120,214,744-120,306,710	IGSF11
nsv869807	copy number variation	87	nstd53	human		NCBI36 chr11: 55,118,273-55,200,744 , GRCh37.p13 chr11: 55,361,697-55,444,168 , GRCh38.p12 chr11: 55,594,221-55,676,692	OR4V1P, OR4P4, 3 more genes
nsv869711	copy number variation	90	nstd53	human		NCBI36 chr4: 69,099,876-69,643,272 , GRCh37.p13 chr: NaN-NaN , GRCh38.p12 chr: NaN-NaN	0
nsv869699	copy number variation	4	nstd53	human		NCBI36 chr4: 69,120,835-69,643,272 , GRCh37.p13 chr: NaN-NaN , GRCh38.p12 chr: NaN-NaN	0
nsv870377	copy number variation	1	nstd53	human		GRCh37.p13 chr3: 162,474,576-162,630,179 , GRCh38.p12 chr3: 162,756,788-162,912,391 , NCBI36 chr3: 163,957,270-164,112,873	0
nsv870114	copy number variation	24	nstd53	human		NCBI36 chr14: 18,537,236-19,478,367 , GRCh38.p12 chr14: 18,690,759-19,940,368 , GRCh37.p13 chr14: 19,467,236-20,408,527	OR4K6P, OR4K5, 54 more genes
nsv870067	copy number variation	15	nstd53	human		NCBI36 chr5: 140,196,541-140,221,835 , GRCh37.p13 chr5: 140,216,357-140,241,651 , GRCh38.p12 chr5: 140,836,772-140,862,066 , GRCh37.p13 chr5\|NW_004775428.1: 71,948-97,242	PCDHA9, PCDHA14, 10 more genes

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