SP51398 AND nstd71 - dbVar - NCBI

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Items: 16

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Number of Variants: 16

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv881140	copy number variation	3	nstd71	human		NCBI36 chr5: 17,762,815-17,812,334 , GRCh37.p13 chr5: 17,727,088-17,776,577 , GRCh38.p12 chr5: 17,726,979-17,776,468	LOC105374666
nsv908486	copy number variation	37	nstd71	human		NCBI36 chr17: 41,814,370-41,922,658 , GRCh37.p13 chr17: 44,458,950-44,566,775 , GRCh38.p12 chr17\|NT_187663.1: 1,118,857-1,181,521	NSF
nsv885483	copy number variation	15	nstd71	human		NCBI36 chr6: 32,653,794-32,673,309 , GRCh37.p13 chr6: 32,545,816-32,565,331 , GRCh38.p12 chr6: 32,578,039-32,597,554	HLA-DRB1
nsv900138	copy number variation	56	nstd71	human		NCBI36 chr13: 56,603,368-56,620,289 , GRCh37.p13 chr13: 57,705,367-57,722,288 , GRCh38.p12 chr13: 57,131,233-57,148,154	PRR20B, PRR20A
nsv893234	copy number variation	15	nstd71	human		NCBI36 chr9: 43,594,114-43,683,382 , GRCh37.p13 chr9: 43,654,118-43,743,386 , GRCh38.p12 chr9: 42,071,003-42,160,271	CNTNAP3B, LOC100420440
nsv896424	copy number variation	1	nstd71	human		NCBI36 chr10: 135,209,148-135,235,772 , GRCh37.p13 chr10: 135,359,158-135,385,782 , GRCh38.p12 chr10: 133,545,654-133,572,278	SYCE1, SPRNP1
nsv879353	copy number variation	96	nstd71	human		NCBI36 chr4: 69,127,630-69,179,871 , GRCh37.p13 chr4: 69,445,035-69,497,276 , GRCh38.p12 chr4: 68,579,317-68,631,558	LOC100132651, LOC100422402, 1 more genes
nsv892146	copy number variation	3	nstd71	human		NCBI36 chr9: 5,290,316-5,330,129 , GRCh37.p13 chr9: 5,300,316-5,340,129 , GRCh38.p12 chr9: 5,300,316-5,340,129	HMGN2P31, RLN2, 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
nsv886732	copy number variation	1	nstd71	human		NCBI36 chr6: 142,332,031-142,577,742 , GRCh37.p13 chr6: 142,290,338-142,536,049 , GRCh38.p12 chr6: 141,969,201-142,214,912	LOC107986654, NMBR, 3 more genes
nsv880213	copy number variation	14	nstd71	human		NCBI36 chr4: 145,129,721-145,259,965 , GRCh37.p13 chr4: 144,910,271-145,040,515 , GRCh38.p12 chr4: 143,989,118-144,119,362	LOC105377460, GYPA, 2 more genes
nsv902807	copy number variation	22	nstd71	human		NCBI36 chr15: 19,031,839-19,212,282 , GRCh37.p13 chr: NaN-NaN , GRCh38.p12 chr15: 20,729,748-21,258,351	NBEAP1, LOC100287357, 22 more genes
nsv913754	copy number variation	1	nstd71	human		NCBI36 chr21: 41,213,548-41,263,464 , GRCh37.p13 chr21: 42,291,678-42,341,594 , GRCh38.p12 chr21: 40,919,752-40,969,668	0
nsv896345	copy number variation	4	nstd71	human		NCBI36 chr10: 135,102,337-135,202,003 , GRCh37.p13 chr10: 135,252,347-135,352,013 , GRCh38.p12 chr10: 133,438,843-133,538,509	LOC105378575, CYP2E1, 4 more genes
nsv903340	copy number variation	3	nstd71	human		NCBI36 chr15: 19,788,917-20,080,112 , GRCh37.p13 chr15: 22,287,553-22,578,748 , GRCh38.p12 chr15: 21,999,602-22,290,797	LOC107983983, , 17 more genes
nsv901323	copy number variation	4	nstd71	human		NCBI36 chr14: 19,272,965-19,492,423 , GRCh37.p13 chr14: 20,203,125-20,422,583 , GRCh38.p12 chr14: 19,734,966-19,954,424	OR4K4P, OR4N2, 10 more genes

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