2-1089-004 AND nstd173 - dbVar - NCBI

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Items: 19

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Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4380463	copy number variation	77	nstd173	human		GRCh37 chr2: 98,118,115-98,162,176 , GRCh38.p12 chr2: 97,501,652-97,545,713	ANKRD36B
nsv4370719	copy number variation	6	nstd173	human		GRCh37 chr6: 152,343,718-152,371,764 , GRCh38.p12 chr6: 152,022,583-152,050,629	ESR1
nsv4375488	copy number variation	51	nstd173	human		GRCh37 chr1: 196,714,810-196,741,354 , GRCh38.p12 chr1: 196,745,680-196,772,224	CFH
nsv4383853	copy number variation	5	nstd173	human		GRCh37 chr8: 57,049,909-57,096,018 , GRCh38.p12 chr8: 56,137,350-56,183,459	PLAG1
nsv4375212	copy number variation	547	nstd173	human		GRCh37 chr1: 72,762,663-72,811,904 , GRCh38.p12 chr1: 72,296,980-72,346,221 , GRCh38.p12 chr1\|NW_018654707.1: 9,247-67,446	RPL31P12, LOC105378797
nsv4367066	copy number variation	60	nstd173	human		GRCh37 chr14: 86,460,915-86,494,554 , GRCh38.p12 chr14: 85,994,571-86,028,210	LINC02316, LINC02328
nsv4384569	copy number variation	2	nstd173	human		GRCh37 chr12: 52,845,924-52,866,028 , GRCh38.p12 chr12: 52,452,140-52,472,244	KRT6B, KRT6C
nsv4383758	copy number variation	118	nstd173	human		GRCh37 chr4: 69,435,889-69,541,963 , GRCh38.p12 chr4: 68,570,171-68,676,245	LOC100422402, UGT2B17, 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
nsv4371067	copy number variation	1	nstd173	human		GRCh37 chr14: 106,329,184-106,740,452 , GRCh38.p12 chr14: 105,862,974-106,283,860 , GRCh38.p12 chr14\|NT_187600.1: 420,111-1,214,078	GOLGA4P2, IGHJ4, 160 more genes
nsv4368214	copy number variation	1	nstd173	human		GRCh37 chr22: 22,740,466-23,258,369 , GRCh38.p12 chr22: 22,386,099-22,916,199	GGTLC2, IGLV3-31, 76 more genes
nsv4374875	copy number variation	271	nstd173	human		GRCh37 chr6: 67,009,023-67,051,189 , GRCh38.p12 chr6: 66,299,130-66,341,296	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
nsv4381353	copy number variation	15	nstd173	human		GRCh37 chr13: 69,242,242-69,264,684 , GRCh38.p12 chr13: 68,668,110-68,690,552	0
nsv4369274	copy number variation	262	nstd173	human		GRCh37 chr2: 35,976,209-35,997,473 , GRCh38.p12 chr2: 35,751,143-35,772,407	0
nsv4374591	copy number variation	15	nstd173	human		GRCh37 chr14: 22,377,905-22,995,123 , GRCh38.p12 chr14: 21,909,724-22,526,154	, TRAV14DV4, 96 more genes
nsv4383095	copy number variation	1	nstd173	human		GRCh37 chrX: 1,356,043-1,523,208 , GRCh38.p12 chrX: 1,237,150-1,404,315	ASMTL-AS1, MIR3690, 11 more genes
nsv4370124	copy number variation	182	nstd173	human		GRCh37 chr7: 142,266,307-142,493,638 , GRCh38.p12 chr7: 142,618,685-142,785,829 , GRCh38.p12 chr7\|NT_187562.1: 656,734-781,128	TRBV27, TRBV21-1, 23 more genes
nsv4373520	copy number variation	108	nstd173	human		GRCh37 chr7: 38,293,950-38,394,857 , GRCh38.p12 chr7: 38,254,349-38,355,256	TARP, TRGJ1, 19 more genes

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