"nstd231"[study] AND "deletion"[variant_type] - dbVar - NCBI

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Items: 13

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Number of Variants: 13

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7099294	copy number variation	1	nstd231	human		GRCh37 chr16: 89,394,004-89,490,401 , GRCh38.p12 chr16: 89,327,596-89,423,993	ANKRD11
nsv7099282	copy number variation	1	nstd231	human		GRCh37 chr7: 130,816,477-130,883,958 , GRCh38.p12 chr7: 131,131,718-131,199,199	MKLN1
nsv7099285	copy number variation	1	nstd231	human		GRCh37 chr11: 99,514,466-99,565,136 , GRCh38.p12 chr11: 99,643,735-99,694,405	CNTN5
nsv7099286	copy number variation	4	nstd231	human		GRCh37 chr11: 99,516,916-99,565,136 , GRCh38.p12 chr11: 99,646,185-99,694,405	CNTN5
nsv7099284	copy number variation	1	nstd231	human		GRCh37 chr10: 34,626,272-34,670,662 , GRCh38.p12 chr10: 34,337,344-34,381,734	PARD3
nsv7099302	copy number variation	6	nstd231	human		GRCh37 chrX: 154,912,942-154,946,932 , GRCh38.p12 chrX: 155,683,281-155,717,271	SPRY3
nsv7099283	copy number variation	1	nstd231	human		GRCh37 chr7: 146,194,570-146,213,280 , GRCh38.p12 chr7: 146,497,478-146,516,188	CNTNAP2
nsv7099299	copy number variation	1	nstd231	human		GRCh37 chrX: 31,458,626-31,463,924 , GRCh38.p12 chrX: 31,440,509-31,445,807	DMD
nsv7099295	copy number variation	1	nstd231	human		GRCh37 chr16: 89,399,270-89,505,521 , GRCh38.p12 chr16: 89,332,862-89,439,113	ANKRD11, LOC101927817
nsv7099300	copy number variation	1	nstd231	human		GRCh37 chrX: 48,224,455-48,242,963 , GRCh38.p12 chrX: 48,365,020-48,383,522	SSX4, LOC101060049
nsv7099275	copy number variation	1	nstd231	human		GRCh37 chr4: 147,519,769-147,548,185 , GRCh38.p12 chr4: 146,598,617-146,627,033	0
nsv7099287	copy number variation	2	nstd231	human		GRCh37 chr13: 73,210,039-73,228,607 , GRCh38.p12 chr13: 72,635,901-72,654,469	0
nsv7099280	copy number variation	1	nstd231	human		GRCh37 chr6: 375,264-385,771 , GRCh38.p12 chr6: 375,264-385,771	0

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