2-1329-002 AND nstd173 - dbVar - NCBI

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Number of Variants: 14

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4367014	copy number variation	172	nstd173	human		GRCh37 chr6: 78,969,104-79,035,184 , GRCh38.p12 chr6: 78,259,387-78,325,467	LOC105377865
nsv4385917	copy number variation	155	nstd173	human		GRCh37 chr2: 98,138,417-98,162,188 , GRCh38.p12 chr2: 97,521,954-97,545,725	ANKRD36B
nsv4375689	copy number variation	34	nstd173	human		GRCh37 chr20: 1,557,189-1,597,997 , GRCh38.p12 chr20: 1,576,543-1,617,351	SIRPB1
nsv4376456	copy number variation	1782	nstd173	human		GRCh37 chr8: 39,246,772-39,386,964 , GRCh38.p12 chr8: 39,389,253-39,529,445	ADAM5, ADAM3A
nsv4378486	copy number variation	188	nstd173	human		GRCh37 chr1: 248,753,184-248,795,289 , GRCh38.p12 chr1: 248,589,883-248,631,988	OR2T10, OR2T11
nsv4373025	copy number variation	7	nstd173	human		GRCh37 chr15: 24,350,856-24,504,770 , GRCh38.p12 chr15: 24,105,709-24,259,623	PWRN2, LOC105370733, 1 more genes
nsv4366010	copy number variation	8	nstd173	human		GRCh37 chr11: 55,376,010-55,452,996 , GRCh38.p12 chr11: 55,608,534-55,685,520	OR4P1P, OR4P4, 3 more genes
nsv4376452	copy number variation	337	nstd173	human		GRCh37 chr17: 34,437,494-34,477,480 , GRCh38.p12 chr17: 36,110,101-36,150,098 , GRCh38.p12 chr17\|NT_187661.1: 64,198-104,195 , GRCh38.p12 chr17\|NT_187614.1: 345,022-385,008	LOC101927369, LOC107985055, 3 more genes
nsv4368821	copy number variation	1373	nstd173	human		GRCh37 chr22: 24,353,749-24,385,040 , GRCh38.p12 chr22\|NT_187633.1: 247,924-279,215	LOC391322, GSTTP2, 3 more genes
nsv4374823	copy number variation	2	nstd173	human		GRCh37 chr20: 55,408,357-55,433,127 , GRCh38.p12 chr20: 56,833,301-56,858,071	0
nsv4372557	copy number variation	42	nstd173	human		GRCh37 chr6: 31,283,853-31,305,152 , GRCh38.p12 chr6: 31,316,076-31,337,375	0
nsv4371390	copy number variation	37	nstd173	human		GRCh37 chr10: 46,966,534-48,174,779 , GRCh38.p12 chr10: 46,157,935-47,923,579	GDF2, RNA5SP311, 54 more genes
nsv4372441	copy number variation	3	nstd173	human		GRCh37 chr8: 48,163,536-48,222,687 , GRCh38.p12 chr: NaN-NaN	0
nsv4381181	copy number variation	1	nstd173	human		GRCh37 chrX: 35,857,241-35,911,077 , GRCh38.p12 chrX: 35,839,124-35,892,960	0

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