MS18465 AND nstd71 - dbVar - NCBI

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Items: 14

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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
nsv884822	copy number variation	2547	nstd71	human		NCBI36 chr6: 32,560,168-32,593,470 , GRCh37.p13 chr6: 32,452,190-32,485,492 , GRCh38.p12 chr6: 32,484,413-32,517,715	HLA-DRB5
nsv909834	copy number variation	44	nstd71	human		NCBI36 chr18: 64,892,426-64,909,808 , GRCh37.p13 chr18: 66,741,446-66,758,828 , GRCh38.p12 chr18: 69,074,209-69,091,591	CCDC102B
nsv891984	copy number variation	3	nstd71	human		NCBI36 chr9: 500,546-638,943 , GRCh37.p13 chr9: 510,546-648,943 , GRCh38.p12 chr9: 510,546-648,943	RNU6-1327P, KANK1
nsv908473	copy number variation	144	nstd71	human		NCBI36 chr17: 41,801,275-41,922,658 , GRCh37.p13 chr17: 44,445,525-44,566,775 , GRCh38.p12 chr17: 46,368,159-46,489,976 , GRCh38.p12 chr17\|NT_187663.1: 1,118,390-1,181,521	NSF, NSFP1
nsv878783	copy number variation	1	nstd71	human		NCBI36 chr4: 28,289,618-28,452,127 , GRCh37.p13 chr4: 28,680,520-28,843,029 , GRCh38.p12 chr4: 28,678,898-28,841,407	RN7SL101P, MESTP3, 1 more genes
nsv892902	copy number variation	16	nstd71	human		NCBI36 chr9: 28,591,613-28,744,535 , GRCh37.p13 chr9: 28,601,613-28,754,535 , GRCh38.p12 chr9: 28,601,615-28,754,537	LINGO2, LOC105376004, 1 more genes
nsv879310	copy number variation	1929	nstd71	human		NCBI36 chr4: 69,076,346-69,179,871 , GRCh37.p13 chr4: 69,393,751-69,497,276 , GRCh38.p12 chr4: 68,528,033-68,631,558	LOC100422402, LOC100132651, 2 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
nsv883934	copy number variation	14	nstd71	human		NCBI36 chr6: 29,989,443-30,005,175 , GRCh37.p13 chr6\|NT_167246.1: 1,175,640-1,191,404 , GRCh37.p13 chr6: 29,881,464-29,897,196 , GRCh38.p12 chr6\|NT_167246.2: 1,170,020-1,185,784 , GRCh38.p12 chr6: 29,913,687-29,929,419	HLA-K, HCG4B, 1 more genes
nsv883570	copy number variation	167	nstd71	human		NCBI36 chr6: 29,957,666-29,972,182 , GRCh37.p13 chr6: 29,849,687-29,864,203 , GRCh38.p12 chr6: 29,881,910-29,896,426	HLA-T, HCG4P7, 1 more genes
nsv883811	copy number variation	81	nstd71	human		NCBI36 chr6: 29,978,470-29,988,619 , GRCh37.p13 chr6\|NT_167246.1: 1,164,662-1,174,816 , GRCh37.p13 chr6: 29,870,491-29,880,640 , GRCh38.p12 chr6\|NT_167246.2: 1,159,042-1,169,196 , GRCh38.p12 chr6: 29,902,714-29,912,863	HLA-A, DDX39BP1, 2 more genes
nsv896349	copy number variation	30	nstd71	human		NCBI36 chr10: 135,102,337-135,235,772 , GRCh37.p13 chr10: 135,252,347-135,385,782 , GRCh38.p12 chr10: 133,438,843-133,572,278	CYP2E1, OR7M1P, 6 more genes
nsv901374	copy number variation	48	nstd71	human		NCBI36 chr14: 19,301,051-19,494,891 , GRCh37.p13 chr14: 20,231,211-20,425,051 , GRCh38.p12 chr14: 19,763,052-19,956,892	LOC100421751, OR4N1P, 9 more genes
nsv905963	copy number variation	12	nstd71	human		NCBI36 chr16: 32,409,337-32,511,911 , GRCh37.p13 chr16: 32,501,836-32,604,410 , GRCh38.p12 chr16: 32,490,515-32,593,089	0

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