IS38634 AND nstd71 - 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
nsv886256	copy number variation	1	nstd71	human		NCBI36 chr6: 79,029,920-79,076,024 , GRCh37.p13 chr6: 78,973,201-79,019,305 , GRCh38.p12 chr6: 78,263,484-78,309,588	LOC105377865
nsv884171	copy number variation	3	nstd71	human		NCBI36 chr6: 31,382,672-31,400,561 , GRCh37.p13 chr6: 31,274,693-31,292,582 , GRCh37.p13 chr6\|NT_167249.1: 2,608,445-2,626,300 , GRCh37.p13 chr6\|NT_167246.1: 2,621,533-2,631,393 , GRCh38.p12 chr6: 31,306,916-31,324,805 , GRCh38.p12 chr6\|NT_167249.2: 2,609,147-2,627,002 , GRCh38.p12 chr6\|NT_167246.2: 2,615,913-2,625,775	LOC112267902
nsv884925	copy number variation	4	nstd71	human		NCBI36 chr6: 32,580,371-32,597,079 , GRCh37.p13 chr6: 32,472,393-32,489,101 , GRCh38.p12 chr6: 32,504,616-32,521,324	HLA-DRB5
nsv890784	copy number variation	129	nstd71	human		NCBI36 chr8: 39,356,825-39,509,376 , GRCh37.p13 chr8: 39,237,668-39,390,219 , GRCh38.p12 chr8: 39,380,149-39,532,700	ADAM3A, ADAM5
nsv899837	copy number variation	61	nstd71	human		NCBI36 chr13: 18,427,644-18,524,818 , GRCh37.p13 chr13: 19,529,644-19,626,818 , GRCh38.p12 chr13: 18,955,504-19,052,678	USP24P1, PHF2P2, 3 more genes
nsv903587	copy number variation	19	nstd71	human		NCBI36 chr15: 21,163,586-21,219,533 , GRCh37.p13 chr15: 23,612,145-23,668,092 , GRCh38.p12 chr15: 23,366,998-23,422,945	LOC105370728, LOC105370726, 1 more genes
nsv871196	copy number variation	88	nstd71	human		NCBI36 chr1: 12,777,429-12,810,136 , GRCh37.p13 chr1: 12,854,842-12,887,549 , GRCh38.p12 chr1: 12,794,693-12,827,690	PRAMEF11, PRAMEF1, 1 more genes
nsv895786	copy number variation	6	nstd71	human		NCBI36 chr10: 81,522,610-81,586,964 , GRCh37.p13 chr10: 81,561,459-81,596,984 , GRCh38.p12 chr10: 79,801,703-79,837,228	LOC642361, NUTM2B-AS1, 1 more genes
nsv915144	copy number variation	37	nstd71	human		NCBI36 chr22: 21,041,786-21,066,291 , GRCh37.p13 chr22: 22,711,786-22,736,291 , GRCh38.p12 chr22: 22,357,438-22,381,922	IGLV1-44, IGLV5-45, 4 more genes
nsv886056	copy number variation	5	nstd71	human		NCBI36 chr6: 67,065,007-67,104,015 , GRCh37.p13 chr6: 67,008,286-67,047,294 , GRCh38.p12 chr6: 66,298,393-66,337,401	0
nsv885736	copy number variation	9	nstd71	human		NCBI36 chr6: 32,989,505-33,006,850 , GRCh37.p13 chr6: 32,881,527-32,898,872 , GRCh37.p13 chr6\|NT_167247.1: 4,218,377-4,235,721 , GRCh38.p12 chr6\|NT_167247.2: 4,212,792-4,230,136 , GRCh38.p12 chr6: 32,913,750-32,931,095	0

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