182134 AND nstd173 - dbVar - NCBI

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Items: 15

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Number of Variants: 15

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4376255	copy number variation	343	nstd173	human		GRCh37 chr2: 98,118,199-98,162,176 , GRCh38.p12 chr2: 97,501,736-97,545,713	ANKRD36B
nsv4376609	copy number variation	40	nstd173	human		GRCh37 chr7: 141,755,372-141,789,964 , GRCh38.p12 chr7: 142,055,572-142,090,164 , GRCh38.p12 chr7\|NT_187562.1: 17,452-52,044	MGAM
nsv4379737	copy number variation	349	nstd173	human		GRCh37 chr1: 169,216,099-169,241,765 , GRCh38.p12 chr1: 169,246,861-169,272,527	NME7
nsv4370571	copy number variation	34	nstd173	human		GRCh37 chr5: 9,901,952-9,926,410 , GRCh38.p12 chr5: 9,901,840-9,926,298	LINC02112
nsv4387580	copy number variation	1	nstd173	human		GRCh37 chr4: 41,454,372-41,477,548 , GRCh38.p12 chr4: 41,452,355-41,475,531	LIMCH1
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
nsv4378128	copy number variation	463	nstd173	human		GRCh37 chr11: 51,337,076-51,376,963 , GRCh38.p12 chr11: 54,742,317-54,782,204	0
nsv4367492	copy number variation	84	nstd173	human		GRCh37 chr4: 161,041,291-161,080,636 , GRCh38.p12 chr4: 160,120,139-160,159,484	0
nsv4381974	copy number variation	9	nstd173	human		GRCh37 chr5: 7,177,338-7,202,635 , GRCh38.p12 chr5: 7,177,225-7,202,522	0
nsv4370854	copy number variation	55	nstd173	human		GRCh37 chr6: 31,280,867-31,305,152 , GRCh38.p12 chr6: 31,313,090-31,337,375	0
nsv4368660	copy number variation	868	nstd173	human		GRCh37 chr6: 103,738,197-103,759,824 , GRCh38.p12 chr6: 103,290,322-103,311,949	0
nsv4380182	copy number variation	1	nstd173	human		GRCh37 chr14: 22,410,495-22,995,123 , GRCh38.p12 chr14: 21,942,304-22,526,154	TRAJ52, TRAV8-6, 93 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
nsv4379398	copy number variation	4	nstd173	human		GRCh37 chr7: 142,338,344-142,486,548 , GRCh38.p12 chr7: 142,630,828-142,778,738 , GRCh38.p12 chr7\|NT_187562.1: 656,734-781,128	TRBVA, MTRNR2L6, 17 more genes
nsv4387226	copy number variation	100	nstd173	human		GRCh37 chr7: 38,293,950-38,387,020 , GRCh38.p12 chr7: 38,254,349-38,347,419	TRGV8, TRGV5P, 18 more genes

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