MS12387 AND nstd71 - dbVar - NCBI

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Number of Variants: 14

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv884818	copy number variation	499	nstd71	human		NCBI36 chr6: 32,560,168-32,591,507 , GRCh37.p13 chr6: 32,452,190-32,483,529 , GRCh38.p12 chr6: 32,484,413-32,515,752	HLA-DRB5
nsv909839	copy number variation	966	nstd71	human		NCBI36 chr18: 64,895,268-64,909,808 , GRCh37.p13 chr18: 66,744,288-66,758,828 , GRCh38.p12 chr18: 69,077,051-69,091,591	CCDC102B
nsv890754	copy number variation	920	nstd71	human		NCBI36 chr8: 39,350,791-39,509,376 , GRCh37.p13 chr8: 39,231,634-39,390,219 , GRCh38.p12 chr8: 39,374,115-39,532,700	ADAM5, ADAM3A
nsv874269	copy number variation	3	nstd71	human		NCBI36 chr2: 73,691,259-73,767,527 , GRCh37.p13 chr2: 73,837,751-73,914,019 , GRCh38.p12 chr2: 73,610,624-73,686,892	ALMS1P1, NAT8
nsv903607	copy number variation	1	nstd71	human		NCBI36 chr15: 21,897,319-22,089,522 , GRCh37.p13 chr15: 24,346,226-24,538,429 , GRCh38.p12 chr15: 24,101,079-24,293,282	LOC105370732, LOC105370733, 2 more genes
nsv908442	copy number variation	4	nstd71	human		NCBI36 chr17: 41,788,595-41,907,421 , GRCh37.p13 chr17: 44,432,855-44,552,105 , GRCh38.p12 chr17\|NT_187663.1: 1,118,390-1,181,521 , GRCh38.p12 chr17: 46,355,489-46,474,739	NSF, NSFP1, 1 more genes
nsv903668	copy number variation	1	nstd71	human		NCBI36 chr15: 22,114,056-22,204,382 , GRCh37.p13 chr15: 24,562,963-24,653,289 , GRCh38.p12 chr15: 24,317,816-24,408,142	LOC105370733, LOC102725165, 1 more genes
nsv903908	copy number variation	4	nstd71	human		NCBI36 chr15: 30,231,488-30,321,329 , GRCh37.p13 chr15: 32,444,196-32,534,037 , GRCh38.p12 chr15: 32,151,995-32,241,836	, CHRNA7, 1 more genes
nsv879254	copy number variation	538	nstd71	human		NCBI36 chr4: 69,047,457-69,179,871 , GRCh37.p13 chr4: 69,364,862-69,497,276 , GRCh38.p12 chr4: 68,499,144-68,631,558	LOC728807, UGT2B29P, 3 more genes
nsv906100	copy number variation	1	nstd71	human		NCBI36 chr16: 32,432,070-32,468,721 , GRCh37.p13 chr16: 32,524,569-32,561,220 , GRCh38.p12 chr16: 32,513,248-32,549,899	0
nsv895272	copy number variation	10	nstd71	human		NCBI36 chr10: 47,013,541-47,454,088 , GRCh37.p13 chr10: 47,689,666-47,934,082 , GRCh38.p12 chr10: 46,172,299-46,398,663	AGAP14P, ANXA8L1, 6 more genes
nsv903065	copy number variation	2	nstd71	human		NCBI36 chr15: 19,341,464-19,407,285 , GRCh37.p13 chr: NaN-NaN , GRCh38.p12 chr15\|NT_187602.1: 203,114-268,890 , GRCh38.p12 chr15\|NT_187382.1: 172,363-238,139	VN1R60P, NF1P9, 5 more genes
nsv903213	copy number variation	198	nstd71	human		NCBI36 chr15: 19,635,853-19,950,423 , GRCh37.p13 chr15: 21,371,194-22,449,059 , GRCh38.p12 chr15: 21,165,865-22,161,108	OR4H6P, OR4Q1P, 49 more genes
nsv875088	copy number variation	3	nstd71	human		NCBI36 chr2: 130,649,378-130,843,631 , GRCh37.p13 chr2: 130,932,908-131,127,161 , GRCh38.p12 chr2: 130,175,335-130,369,588	RHOQP3, TEKT4P3, 22 more genes

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