"nstd98"[study] AND "deletion"[variant_type] - dbVar - NCBI

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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
nsv1067814	copy number variation	1	nstd98	human		GRCh37 chr11: 130,434,794-130,623,967 , GRCh38.p12 chr11: 130,564,899-130,754,072	LINC02873, MIR8052, 1 more genes
nsv1067815	copy number variation	1	nstd98	human		GRCh37 chr11: 130,434,721-130,623,850 , GRCh38.p12 chr11: 130,564,826-130,753,955	LINC02873, MIR8052, 1 more genes
nsv1067813	copy number variation	1	nstd98	human		GRCh37 chr2: 77,318,421-78,195,294 , GRCh38.p12 chr2: 77,091,295-77,968,168	LRRTM4, RPL38P2, 5 more genes
nsv1067822	copy number variation	2	nstd98	human		GRCh37 chr2: 77,318,677-78,195,473 , GRCh38.p12 chr2: 77,091,551-77,968,347	LRRTM4, RPL38P2, 5 more genes
nsv1067810	copy number variation	1	nstd98	human		GRCh37 chr3: 112,138,686-115,514,746 , GRCh38.p12 chr3: 112,419,839-115,795,899	ATP6V1A, DRD3, 56 more genes
nsv1067819	copy number variation	1	nstd98	human		GRCh37 chr3: 112,139,369-115,515,376 , GRCh38.p12 chr3: 112,420,522-115,796,529	ATP6V1A, DRD3, 56 more genes
nsv1067812	copy number variation	1	nstd98	human		GRCh37 chr3: 112,139,553-115,515,552 , GRCh38.p12 chr3: 112,420,706-115,796,705	ATP6V1A, DRD3, 56 more genes
nsv1067824	copy number variation	1	nstd98	human		GRCh37 chr3: 112,139,023-115,515,016 , GRCh38.p12 chr3: 112,420,176-115,796,169	ATP6V1A, DRD3, 56 more genes
nsv1067818	copy number variation	2	nstd98	human		GRCh37 chr3: 112,138,807-115,514,798 , GRCh38.p12 chr3: 112,419,960-115,795,951	ATP6V1A, DRD3, 56 more genes
nsv1067825	copy number variation	1	nstd98	human		GRCh37 chr3: 112,139,311-115,515,278 , GRCh38.p12 chr3: 112,420,464-115,796,431	ATP6V1A, DRD3, 56 more genes
nsv1067811	copy number variation	1	nstd98	human		GRCh37 chr3: 112,139,977-115,515,927 , GRCh38.p12 chr3: 112,421,130-115,797,080	ATP6V1A, DRD3, 56 more genes
nsv1067816	copy number variation	1	nstd98	human		GRCh37 chr1: 222,150,405-223,201,865 , GRCh38.p12 chr1: 221,977,063-223,028,523	TAF1A, AIDA, 20 more genes
nsv1067820	copy number variation	1	nstd98	human		GRCh37 chr1: 222,150,567-223,201,919 , GRCh38.p12 chr1: 221,977,225-223,028,577	TAF1A, AIDA, 20 more genes

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