MS16192 AND nstd71 - dbVar - NCBI

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Items: 8

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Number of Variants: 8

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv874909	copy number variation	74	nstd71	human		NCBI36 chr2: 115,231,523-115,253,261 , GRCh37.p13 chr2: 115,515,053-115,536,791 , GRCh38.p12 chr2: 114,757,476-114,779,214	DPP10
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
nsv911913	copy number variation	63	nstd71	human		NCBI36 chr19: 48,060,801-48,166,539 , GRCh37.p13 chr19: 43,368,961-43,474,699 , GRCh38.p12 chr19: 42,864,809-42,970,547	PSG1, CEACAMP7, 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
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
nsv908379	copy number variation	346	nstd71	human		NCBI36 chr17: 41,775,690-41,922,658 , GRCh37.p13 chr17: 44,419,932-44,566,775 , GRCh38.p12 chr17: 46,342,566-46,489,976	ARL17B, NSFP1, 1 more genes
nsv894694	copy number variation	1	nstd71	human		NCBI36 chr10: 104,779-220,625 , GRCh37.p13 chr10: 114,779-224,405 , GRCh37.p13 chr10\|NW_003571043.1: 58,839-168,465 , GRCh38.p12 chr10: 68,839-184,685	ZMYND11, RNA5SP297, 2 more genes

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