MS25839 AND nstd71 - dbVar - NCBI

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Items: 15

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Number of Variants: 15

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv898302	copy number variation	16	nstd71	human		NCBI36 chr11: 99,079,081-99,103,335 , GRCh37.p13 chr11: 99,573,871-99,598,125 , GRCh38.p12 chr11: 99,703,140-99,727,394	CNTN5
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
nsv905469	copy number variation	2	nstd71	human		NCBI36 chr16: 16,505,578-16,767,302 , GRCh37.p13 chr16: 16,598,077-16,859,801 , GRCh38.p12 chr16\|NT_187607.1: 2,165,280-2,426,878 , GRCh38.p12 chr16: 16,504,220-16,765,944	LOC100133127
nsv909951	copy number variation	1	nstd71	human		NCBI36 chr18: 73,336,488-73,391,251 , GRCh37.p13 chr18: 75,207,500-75,262,263 , GRCh38.p12 chr18: 77,495,544-77,550,307	LOC107985172
nsv912335	copy number variation	19	nstd71	human		NCBI36 chr19: 58,023,726-58,065,844 , GRCh37.p13 chr19: 53,331,914-53,374,032 , GRCh38.p12 chr19: 52,828,661-52,870,779	ZNF320, ZNF468
nsv892894	copy number variation	3	nstd71	human		NCBI36 chr9: 28,552,256-28,697,299 , GRCh37.p13 chr9: 28,562,256-28,707,299 , GRCh38.p12 chr9: 28,562,258-28,707,301	LOC105376003, LOC105376004, 2 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
nsv889118	copy number variation	1	nstd71	human		NCBI36 chr7: 120,470,987-120,588,073 , GRCh37.p13 chr7: 120,683,751-120,800,837 , GRCh38.p12 chr7: 121,043,697-121,160,783	CPED1, RNA5SP241, 1 more genes
nsv896449	copy number variation	1	nstd71	human		NCBI36 chr11: 226,871-239,097 , GRCh37.p13 chr11: 236,871-249,097 , GRCh38.p12 chr11: 236,871-249,097	PSMD13, LOC100420679, 1 more genes
nsv893282	copy number variation	74	nstd71	human		NCBI36 chr9: 43,641,682-44,683,090 , GRCh37.p13 chr9: 43,701,686-44,743,094 , GRCh38.p12 chr9: 41,912,139-42,974,549	CYP4F60P, RBPJP6, 30 more genes
nsv905552	copy number variation	1	nstd71	human		NCBI36 chr16: 18,539,600-18,687,337 , GRCh37.p13 chr16: 18,632,099-18,779,836 , GRCh38.p12 chr16: 18,620,777-18,768,514	0
nsv895538	copy number variation	101	nstd71	human		NCBI36 chr10: 58,562,281-58,608,558 , GRCh37.p13 chr10: 58,892,275-58,938,552 , GRCh38.p12 chr10: 57,132,515-57,178,792	0
nsv903992	copy number variation	6	nstd71	human		NCBI36 chr15: 32,447,708-32,631,865 , GRCh37.p13 chr15: 34,660,416-34,844,573 , GRCh38.p12 chr15: 34,368,215-34,552,372	GOLGA8B, LOC100422491, 7 more genes
nsv903228	copy number variation	62	nstd71	human		NCBI36 chr15: 19,635,853-19,993,878 , GRCh37.p13 chr15: 21,371,194-22,492,514 , GRCh38.p12 chr15: 21,165,865-22,204,563	LOC642131, IGHV1OR15-4, 52 more genes
nsv906153	copy number variation	1	nstd71	human		NCBI36 chr16: 32,437,908-32,502,614 , GRCh37.p13 chr16: 32,530,407-32,595,113 , GRCh38.p12 chr16: 32,519,086-32,583,792	0

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