MS26069 AND nstd71 - dbVar - NCBI

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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
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
nsv908940	copy number variation	1	nstd71	human		NCBI36 chr17: 74,879,587-74,905,632 , GRCh37.p13 chr17: 77,367,992-77,394,037 , GRCh38.p12 chr17: 79,371,910-79,397,955	RBFOX3
nsv890751	copy number variation	169	nstd71	human		NCBI36 chr8: 39,350,791-39,497,557 , GRCh37.p13 chr8: 39,231,634-39,378,400 , GRCh38.p12 chr8: 39,374,115-39,520,881	ADAM5, ADAM3A
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
nsv897976	copy number variation	1	nstd71	human		NCBI36 chr11: 81,150,420-81,786,573 , GRCh37.p13 chr11: 81,472,772-82,108,925 , GRCh38.p12 chr11: 81,761,730-82,397,883	, MIR4300, 1 more genes
nsv874634	copy number variation	114	nstd71	human		NCBI36 chr2: 89,721,421-89,911,010 , GRCh37.p13 chr2: 90,084,116-90,273,705 , GRCh38.p12 chr2: 90,045,284-90,234,838	IGKV3D-15, IGKV1D-16, 14 more genes
nsv874831	copy number variation	4	nstd71	human		NCBI36 chr2: 110,264,613-111,021,091 , GRCh37.p13 chr2: 110,907,324-111,334,482 , GRCh38.p12 chr2: 110,149,747-110,576,877	MTLN, LOC100288570, 15 more genes
nsv902539	copy number variation	5	nstd71	human		NCBI36 chr14: 105,118,950-105,217,427 , GRCh37.p13 chr14\|NW_004166863.1: 244,735-343,212 , GRCh37.p13 chr14: 106,047,905-106,146,382 , GRCh38.p12 chr14: 105,605,043-105,680,045 , GRCh38.p12 chr14\|NT_187600.1: 72,812-147,814	ELK2AP, IGHG4, 8 more genes

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