208032 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
nsv4379109	copy number variation	1337	nstd173	human		GRCh37 chr20: 1,560,774-1,597,997 , GRCh38.p12 chr20: 1,580,128-1,617,351	SIRPB1
nsv4371674	copy number variation	102	nstd173	human		GRCh37 chr3: 89,394,610-89,419,375 , GRCh38.p12 chr3: 89,345,460-89,370,225	EPHA3
nsv4384545	copy number variation	1	nstd173	human		GRCh37 chr4: 80,856,636-80,882,533 , GRCh38.p12 chr4: 79,935,482-79,961,379	ANTXR2
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
nsv4371450	copy number variation	57	nstd173	human		GRCh37 chr12: 2,235,941-2,257,920 , GRCh38.p12 chr12: 2,126,775-2,148,754 , GRCh38.p12 chr12\|NW_018654718.1: 468,919-490,898	LOC107984131, CACNA1C
nsv4380199	copy number variation	2	nstd173	human		GRCh37 chr2: 13,202,931-13,282,921 , GRCh38.p12 chr2: 13,062,806-13,142,796	LOC105373436, LOC105373484
nsv4381562	copy number variation	367	nstd173	human		GRCh37 chr11: 55,374,019-55,453,008 , GRCh38.p12 chr11: 55,606,543-55,685,532	OR4P1P, OR4C6, 3 more genes
nsv4375232	copy number variation	423	nstd173	human		GRCh37 chr5: 180,375,302-180,430,801 , GRCh38.p12 chr5: 180,948,302-181,003,801	BTNL8, LOC100128762, 3 more genes
nsv4385047	copy number variation	40	nstd173	human		GRCh37 chr4: 69,435,889-69,544,335 , GRCh38.p12 chr4: 68,570,171-68,678,617	UGT2B15, LOC728807, 3 more genes
nsv4369627	copy number variation	2	nstd173	human		GRCh37 chr15: 24,350,856-24,782,266 , GRCh38.p12 chr15: 24,105,709-24,537,119	PWRN2, PWRN3, 4 more genes
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
nsv4382392	copy number variation	421	nstd173	human		GRCh37 chr3: 65,185,849-65,210,375 , GRCh38.p12 chr3: 65,200,174-65,224,700	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
nsv4381412	copy number variation	3	nstd173	human		GRCh37 chr21: 15,006,458-15,155,629 , GRCh38.p12 chr21: 13,634,137-13,783,308	LONRF2P5, TERF1P1, 8 more genes
nsv4379973	copy number variation	66	nstd173	human		GRCh37 chr5: 676,873-821,699 , GRCh38.p12 chr5: 676,758-821,584	ZDHHC11B, , 4 more genes
nsv4380296	copy number variation	3	nstd173	human		GRCh37 chrX: 168,547-155,233,756 , GRCh38.p12 chrX: 251,880-156,004,091	RPL31P63, BCYRN1P1, 2192 more genes
nsv4371776	copy number variation	1	nstd173	human		GRCh37 chr14: 22,441,010-22,974,280 , GRCh38.p12 chr14: 21,972,781-22,505,293	TRAV8-7, TRAJ42, 73 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
nsv4367417	copy number variation	12	nstd173	human		GRCh37 chr7: 38,295,932-38,356,732 , GRCh38.p12 chr7: 38,256,331-38,317,131	TARP, TRGJP1, 11 more genes

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