CONTROL_81 AND nstd53 - 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
nsv869730	copy number variation	122	nstd53	human		GRCh38.p12 chr8: 39,377,532-39,528,580 , NCBI36 chr8: 39,354,208-39,505,256 , GRCh37.p13 chr8: 39,235,051-39,386,099	ADAM3A, ADAM5
nsv869574	copy number variation	8	nstd53	human		GRCh38.p12 chr10: 133,475,375-133,558,930 , NCBI36 chr10: 135,138,869-135,222,424 , GRCh37.p13 chr10: 135,288,879-135,372,434	CYP2E1, OR7M1P, 3 more genes
nsv869651	copy number variation	15	nstd53	human		NCBI36 chr15: 32,514,998-32,664,506 , GRCh38.p12 chr15: 34,435,505-34,585,013 , GRCh37.p13 chr15: 34,727,706-34,877,214	GOLGA8A, FSCN1P1, 5 more genes
nsv869577	copy number variation	64	nstd53	human		NCBI36 chr15: 18,867,344-19,943,194 , GRCh38.p12 chr15: 20,402,077-22,153,879 , GRCh37.p13 chr15: 20,607,330-22,441,830	NBEAP1, OR4H6P, 78 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
nsv869818	copy number variation	1	nstd53	human		NCBI36 chr1: 16,817,580-17,124,554 , GRCh38.p12 chr1: 16,618,498-16,925,472 , GRCh37.p13 chr1: 16,944,993-17,251,967	RNU1-4, TRE-TTC3-1, 24 more genes
nsv869849	copy number variation	3	nstd53	human		GRCh38.p12 chr6: 167,942,437-168,187,972 , NCBI36 chr6: 168,085,966-168,331,501 , GRCh37.p13 chr6: 168,343,117-168,588,652	KIF25, AFDN, 5 more genes
nsv870029	copy number variation	3	nstd53	human		GRCh37.p13 chr3: 195,354,183-195,454,454 , GRCh38.p12 chr3: 195,627,312-195,727,583 , NCBI36 chr3: 196,835,472-196,940,125 , GRCh38.p12 chr3\|NT_187649.1: 67,117-139,787 , GRCh38.p12 chr3\|NT_187688.1: 67,117-140,349 , GRCh38.p12 chr3\|NT_187690.1: 67,126-141,061 , GRCh38.p12 chr3\|NT_187691.1: 67,287-142,498 , GRCh38.p12 chr3\|NT_187678.1: 68,461-143,431 , GRCh38.p12 chr3\|NT_187689.1: 23,110-98,080 , GRCh38.p12 chr3\|NT_187532.1: 23,110-98,080	MUC20, MIR570HG, 7 more genes
nsv870083	copy number variation	2	nstd53	human		NCBI36 chr1: 120,867,794-141,559,466 , GRCh37.p13 chr1: 121,166,271-142,617,943 , GRCh38.p12 chr: NaN-NaN	0
nsv869913	copy number variation	7	nstd53	human		GRCh38.p12 chr10: 45,674,428-47,923,579 , NCBI36 chr10: 45,489,882-47,161,232 , GRCh37.p13 chr10: 46,169,876-47,691,226 , GRCh37.p13 chr10\|NW_003871068.1: 1-2,010,264	CTSLP2, GDF2, 71 more genes
nsv869884	copy number variation	1	nstd53	human		NCBI36 chr16: 34,329,577-34,602,318 , GRCh38.p12 chr16: 35,237,705-35,510,446 , GRCh37.p13 chr16: 34,472,076-34,744,817	FRG2DP, LINC01566, 25 more genes

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