DB86 AND nstd158 - 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
nsv3168509	copy number variation	1	nstd158	human		GRCh37 chr11: 88,286,803-88,287,589 , GRCh38.p12 chr11: 88,553,635-88,554,421	GRM5
nsv3169124	copy number variation	1	nstd158	human		GRCh37 chr3: 81,745,301-81,875,104 , GRCh38.p12 chr3: 81,696,150-81,825,953	GBE1
nsv3167918	inversion	1	nstd158	human		GRCh37 chr11: 87,790,951-87,792,325 , GRCh38.p12 chr11: 88,057,783-88,059,157	RAB38
nsv3169326	translocation	1	nstd158	human		GRCh37 chr22: 33,520,316-33,520,370 , GRCh37 chr6\|NT_167248.1: 1,261,568-1,261,622 , GRCh38.p12 chr22: 33,124,330-33,124,384 , GRCh38.p12 chr6\|NT_167248.2: 1,255,972-1,256,026	POLR1HASP
nsv3167908	copy number variation	1	nstd158	human		GRCh38.p12 chr1: 56,607,099-56,687,788 , GRCh37 chr1: 57,072,772-57,153,461	PRKAA2, LOC101929935
nsv3168640	translocation	1	nstd158	human		GRCh38.p12 chr16: 80,878,197-80,879,407 , GRCh37 chr16: 80,912,094-80,913,304 , GRCh37 chr3: 82,108,906-82,110,116 , GRCh38.p12 chr3: 82,059,755-82,060,965	ARLNC1, LINC02008
nsv3168144	copy number variation	1	nstd158	human		GRCh37 chr5: 177,428,510-177,857,269 , GRCh38.p12 chr5: 178,001,509-178,430,268	HNRNPAB, N4BP3, 15 more genes
nsv3168375	copy number variation	1	nstd158	human		GRCh37 chrX: 7,369,854-7,405,329 , GRCh38.p12 chrX: 7,451,813-7,487,288	0
nsv3169155	copy number variation	1	nstd158	human		GRCh38.p12 chr9: 134,763,771-137,911,686 , GRCh37 chr9: 137,655,617-140,806,138	ABCA2, C8G, 155 more genes
nsv3167920	copy number variation	1	nstd158	human		GRCh37 chr3: 197,112,509-197,115,461 , GRCh38.p12 chr3: 197,385,638-197,388,590	0
nsv3168971	inversion	1	nstd158	human		GRCh37 chr5: 175,827,703-177,412,420 , GRCh38.p12 chr5: 176,400,702-177,985,419	CLTB, DBN1, 52 more genes
nsv3169314	inversion	1	nstd158	human		GRCh37 chr13: 89,013,062-89,021,924 , GRCh38.p12 chr13: 88,360,807-88,369,669	0

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