MS11886 AND nstd71 - dbVar - NCBI

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Number of Variants: 7

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv889261	copy number variation	57	nstd71	human		NCBI36 chr7: 141,410,335-141,439,888 , GRCh37.p13 chr7\|NW_003571040.1: 206,017-235,570 , GRCh37.p13 chr7: 141,763,866-141,793,419 , GRCh38.p12 chr7\|NT_187562.1: 25,946-55,499 , GRCh38.p12 chr7: 142,064,066-142,093,619	MGAM
nsv899931	copy number variation	1	nstd71	human		NCBI36 chr13: 23,478,540-23,528,003 , GRCh37.p13 chr13: 24,580,540-24,630,003 , GRCh38.p12 chr13: 24,006,401-24,055,864	SPATA13
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
nsv911379	copy number variation	30	nstd71	human		NCBI36 chr19: 20,413,668-20,507,068 , GRCh37.p13 chr19\|NW_003571053.2: 356,275-449,675 , GRCh37.p13 chr19: 20,621,828-20,715,228 , GRCh38.p12 chr19: 20,439,022-20,532,422	LOC105372317, LOC105372316, 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
nsv871974	copy number variation	3	nstd71	human		NCBI36 chr1: 103,930,296-104,048,591 , GRCh37.p13 chr1: 104,128,773-104,247,068 , GRCh38.p12 chr1: 103,586,151-103,704,446	AMY2A, LOC105378878, 2 more genes
nsv875067	copy number variation	9	nstd71	human		NCBI36 chr2: 130,554,394-130,843,631 , GRCh37.p13 chr2: 130,837,924-131,127,161 , GRCh38.p12 chr2: 130,080,351-130,369,588	PTPN18, MZT2B, 27 more genes

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MS11886 AND nstd71 (8)
dbVar

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