SP81387 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
nsv881606	copy number variation	2	nstd71	human		NCBI36 chr4: 171,877,258-171,997,084 , GRCh37.p13 chr4: 171,640,683-171,760,509 , GRCh38.p12 chr4: 170,719,532-170,839,358	LINC02382
nsv912739	copy number variation	4	nstd71	human		NCBI36 chr20: 14,725,701-14,778,453 , GRCh37.p13 chr20: 14,777,701-14,830,453 , GRCh38.p12 chr20: 14,797,055-14,849,807	MACROD2
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
nsv893239	copy number variation	2	nstd71	human		NCBI36 chr9: 43,594,114-43,730,292 , GRCh37.p13 chr9: 43,654,118-43,790,296 , GRCh38.p12 chr9: 42,024,093-42,160,271	CNTNAP3B, LOC100420440
nsv885392	copy number variation	23	nstd71	human		NCBI36 chr6: 32,638,176-32,660,003 , GRCh37.p13 chr6: 32,530,198-32,552,025 , GRCh38.p12 chr6: 32,562,421-32,584,248	RNU1-152P, HLA-DRB1
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
nsv882104	copy number variation	1	nstd71	human		NCBI36 chr5: 70,261,872-70,351,828 , GRCh37.p13 chr5: 70,226,116-70,316,072 , GRCh38.p12 chr5: 70,930,289-71,020,245	LOC112267942, NAIP, 1 more genes
nsv898478	copy number variation	13	nstd71	human		NCBI36 chr11: 133,654,284-133,714,118 , GRCh37.p13 chr11: 134,149,074-134,208,908 , GRCh38.p12 chr11: 134,279,180-134,339,014	GLB1L2, LOC100421417, 1 more genes
nsv881870	copy number variation	38	nstd71	human		NCBI36 chr5: 69,319,133-69,436,209 , GRCh37.p13 chr5: 69,283,377-69,400,453 , GRCh38.p12 chr5\|NT_187651.1: 243,313-329,959 , GRCh38.p12 chr5: 69,987,550-70,104,626	SMN2, LOC105369228, 5 more genes
nsv881742	copy number variation	4	nstd71	human		NCBI36 chr5: 63,715,205-63,807,817 , GRCh37.p13 chr5: 63,679,449-63,772,061 , GRCh38.p12 chr5: 64,383,622-64,476,234	0

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