192223 AND nstd173 - dbVar - NCBI

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Number of Variants: 18

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4384074	copy number variation	18	nstd173	human		GRCh37 chr11: 49,710,704-49,758,260 , GRCh38.p12 chr11: 49,689,152-49,736,708 , GRCh38.p12 chr11\|NW_019805495.1: 153,334-200,857	GRM5P1
nsv4371509	copy number variation	47	nstd173	human		GRCh37 chr10: 124,358,181-124,382,444 , GRCh38.p12 chr10: 122,598,665-122,622,928	DMBT1
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
nsv4372764	copy number variation	13	nstd173	human		GRCh37 chr6: 124,432,122-124,470,365 , GRCh38.p12 chr6: 124,110,977-124,149,220	NKAIN2
nsv4369101	copy number variation	83	nstd173	human		GRCh37 chr11: 18,941,197-18,962,398 , GRCh38.p12 chr11: 18,919,650-18,940,851	MRGPRX1
nsv4373483	copy number variation	30	nstd173	human		GRCh37 chr3: 46,793,364-46,849,588 , GRCh38.p12 chr3: 46,751,874-46,808,098	PRSS43P, PRSS44P
nsv4365971	copy number variation	432	nstd173	human		GRCh37 chr1: 248,753,196-248,795,289 , GRCh38.p12 chr1: 248,589,895-248,631,988	OR2T10, OR2T11
nsv4381473	copy number variation	1	nstd173	human		GRCh37 chr17: 807,682-831,589 , GRCh38.p12 chr17: 904,442-928,349	NXN, LOC101927727
nsv4366414	copy number variation	36	nstd173	human		GRCh37 chr1: 72,756,112-72,812,440 , GRCh38.p12 chr1: 72,290,429-72,346,757 , GRCh38.p12 chr1\|NW_018654707.1: 2,696-67,982	RPL31P12, LOC105378797
nsv4370277	copy number variation	687	nstd173	human		GRCh37 chr5: 180,378,754-180,430,789 , GRCh38.p12 chr5: 180,951,754-181,003,789	BTNL8, ARPP19P1, 3 more genes
nsv4372487	copy number variation	231	nstd173	human		GRCh37 chr12: 11,219,930-11,251,705 , GRCh38.p12 chr12: 11,067,331-11,099,106	TAS2R64P, PRH1, 3 more genes
nsv4366946	copy number variation	59	nstd173	human		GRCh37 chr14: 106,880,556-106,924,839 , GRCh38.p12 chr14: 106,424,650-106,468,915 , GRCh38.p12 chr14\|NT_187600.1: 916,329-960,594	IGH, IGHVII-40-1, 5 more genes
nsv4384501	copy number variation	242	nstd173	human		GRCh37 chr16: 19,945,795-19,965,942 , GRCh38.p12 chr16: 19,934,473-19,954,620	0
nsv4370707	copy number variation	2	nstd173	human		GRCh37 chr14: 22,392,639-22,974,280 , GRCh38.p12 chr14: 21,924,463-22,505,293	TRAJ48, TRAV22, 77 more genes
nsv4385415	copy number variation	63	nstd173	human		GRCh37 chr17: 44,212,824-44,784,639 , GRCh38.p12 chr17: 46,135,458-46,707,273 , GRCh38.p12 chr17\|NT_187663.1: 837,565-1,226,699	DND1P2, RN7SL656P, 14 more genes
nsv4372404	copy number variation	32	nstd173	human		GRCh37 chr7: 142,338,344-142,493,638 , GRCh38.p12 chr7: 142,630,828-142,785,829 , GRCh38.p12 chr7\|NT_187562.1: 656,734-781,128	TRBV27, PRSS3P2, 21 more genes
nsv4380787	copy number variation	76	nstd173	human		GRCh37 chr7: 38,294,983-38,387,020 , GRCh38.p12 chr7: 38,255,382-38,347,419	TRG, TRGV5P, 18 more genes
nsv4368476	copy number variation	44	nstd173	human		GRCh37 chr14: 107,144,399-107,184,582 , GRCh38.p12 chr14: 106,688,382-106,776,343	IGHV2-70, IGHV1-69D, 9 more genes

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