"nstd220"[study] AND "copy number loss"[variant_type] - dbVar - NCBI

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Number of Variants: 12

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6314786	copy number variation	1	nstd220	human		GRCh37 chrX: 2,795,214-17,648,380 , GRCh38.p12 chrX: 2,877,173-17,630,260	AMELX, SHROOM2, 156 more genes
nsv6314783	copy number variation	1	nstd220	human		GRCh37 chrX: 2,795,214-16,240,667 , GRCh38.p12 chrX: 2,877,173-16,222,544	AMELX, SHROOM2, 137 more genes
nsv6314781	copy number variation	1	nstd220	human		GRCh38.p12 chr4: 181,774,580-188,158,025 , GRCh37 chr4: 182,695,733-189,079,179	SLC25A4, CASP3, 117 more genes
nsv6314782	copy number variation	1	nstd220	human		GRCh38.p12 chr22: 21,351,861-24,248,764 , GRCh37 chr22: 21,706,150-24,644,732	ASLP1, BCR, 195 more genes
nsv6314785	copy number variation	1	nstd220	human		GRCh38.p12 chr16: 15,301,199-18,107,076 , GRCh37 chr16: 15,395,056-18,200,933 , GRCh38.p12 chr16\|NT_187607.1: 1,015,619-2,659,700	ABCC6, ABCC1, 38 more genes
nsv6314790	copy number variation	1	nstd220	human		GRCh37 chr17: 34,710,859-36,306,985 , GRCh38.p12 chr17: 36,446,545-38,150,935 , GRCh38.p12 chr17\|NT_187614.1: 694,163-2,186,050	ACACA, LHX1, 49 more genes
nsv6314789	copy number variation	1	nstd220	human		GRCh37 chrX: 6,472,218-8,150,233 , GRCh38.p12 chrX: 6,554,177-8,182,192	STS, PUDP, 9 more genes
nsv6314777	copy number variation	1	nstd220	human		GRCh38.p12 chr2: 110,718,642-112,337,698 , GRCh37 chr2: 111,476,219-113,095,275	BCL2L11, MERTK, 25 more genes
nsv6314787	copy number variation	1	nstd220	human		GRCh37 chrX: 6,445,119-8,104,085 , GRCh38.p12 chrX: 6,527,078-8,136,044	STS, PUDP, 8 more genes
nsv6314779	copy number variation	1	nstd220	human		GRCh38.p12 chr16: 15,018,282-16,467,270 , GRCh37 chr16: 15,112,139-16,561,127 , GRCh38.p12 chr16\|NT_187607.1: 857,626-2,128,327	ABCC6, ABCC1, 45 more genes
nsv6314792	copy number variation	1	nstd220	human		GRCh37 chr17: 14,161,233-15,458,439 , GRCh38.p12 chr17: 14,257,916-15,555,125	PMP22, HS3ST3B1, 22 more genes
nsv6314784	copy number variation	1	nstd220	human		GRCh38.p12 chr16: 15,048,956-16,334,780 , GRCh37 chr16: 15,142,813-16,428,637 , GRCh38.p12 chr16\|NT_187607.1: 1,015,619-1,993,961	ABCC6, ABCC1, 35 more genes

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