"nstd164"[study] AND "copy number loss"[variant_type] - dbVar - NCBI

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Number of Variants: 10

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3418829	copy number variation	1	nstd164	human		GRCh37 chr17: 58,857,889-58,868,337 , GRCh38.p12 chr17: 60,780,528-60,790,976	BCAS3
nsv3418823	copy number variation	2	nstd164	human		GRCh37 chr17: 59,542,891-59,551,503 , GRCh38.p12 chr17: 61,465,530-61,474,142	TBX4
nsv3418821	copy number variation	2	nstd164	human		GRCh37 chr5: 43,957,152-46,135,209 , GRCh38.p12 chr5: 43,957,050-46,135,107	FGF10, MRPS30, 6 more genes
nsv3418824	copy number variation	1	nstd164	human		GRCh37 chr5: 42,985,023-45,244,787 , GRCh38.p12 chr5: 42,984,921-45,244,685	FGF10, HMGCS1, 29 more genes
nsv3418826	copy number variation	1	nstd164	human		GRCh37 chr17: 58,086,876-60,344,516 , GRCh38.p12 chr17: 60,009,515-62,267,155	CA4, TBX2, 46 more genes
nsv3418827	copy number variation	1	nstd164	human		GRCh37 chr17: 58,089,454-60,346,711 , GRCh38.p12 chr17: 60,012,093-62,269,350	CA4, TBX2, 46 more genes
nsv3418822	copy number variation	2	nstd164	human		GRCh37 chr17: 58,088,933-60,346,028 , GRCh38.p12 chr17: 60,011,572-62,268,667	CA4, TBX2, 46 more genes
nsv3418828	copy number variation	1	nstd164	human		GRCh37 chr17: 58,090,283-60,347,230 , GRCh38.p12 chr17: 60,012,922-62,269,869	CA4, TBX2, 46 more genes
nsv3418830	copy number variation	1	nstd164	human		GRCh37 chr17: 59,272,842-61,392,997 , GRCh38.p12 chr17: 61,195,481-63,315,636	TBX2, TBX4, 39 more genes
nsv3418825	copy number variation	1	nstd164	human		GRCh37 chr17: 58,167,485-60,174,066 , GRCh38.p12 chr17: 60,090,124-62,096,705	CA4, TBX2, 35 more genes

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