OCD142-0625-7951-1 AND nstd173 - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
nsv4376284	copy number variation	379	nstd173	human	GRCh37 chr14: 41,608,616-41,657,457 , GRCh38.p12 chr14: 41,139,413-41,188,254	LINC02315
nsv4376921	copy number variation	59	nstd173	human	GRCh37 chr2: 98,118,199-98,161,960 , GRCh38.p12 chr2: 97,501,736-97,545,497	ANKRD36B
nsv4369227	copy number variation	203	nstd173	human	GRCh37 chr1: 72,771,366-72,811,904 , GRCh38.p12 chr1: 72,305,683-72,346,221 , GRCh38.p12 chr1\|NW_018654707.1: 17,950-67,446	LOC105378797
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
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
nsv4380957	copy number variation	3	nstd173	human	GRCh37 chr10: 45,210,690-45,366,907 , GRCh38.p12 chr10: 44,715,242-44,871,459	TMEM72-AS1, EIF2AP4
nsv4388035	copy number variation	283	nstd173	human	GRCh37 chr1: 104,109,088-104,132,506 , GRCh38.p12 chr1: 103,566,466-103,589,884	AMY2B, ACTG1P4
nsv4373753	copy number variation	13	nstd173	human	GRCh37 chr1: 1,616,990-1,672,602 , GRCh38.p12 chr1: 1,685,551-1,741,163	LOC100129381, CDK11A, 3 more genes
nsv4386129	copy number variation	134	nstd173	human	GRCh37 chr17: 34,439,977-34,477,480 , GRCh38.p12 chr17: 36,112,584-36,150,098 , GRCh38.p12 chr17\|NT_187661.1: 66,681-104,195 , GRCh38.p12 chr17\|NT_187614.1: 347,505-385,008	LOC101927369, LOC100419980, 2 more genes
nsv4380214	copy number variation	10	nstd173	human	GRCh37 chr19: 20,598,430-20,716,388 , GRCh38.p12 chr19: 20,415,624-20,533,582	ZNF826P, ZNF737, 4 more genes
nsv4372749	copy number variation	3	nstd173	human	GRCh37 chr14: 106,071,832-106,223,587 , GRCh38.p12 chr14: 105,605,495-105,757,250 , GRCh38.p12 chr14\|NT_187600.1: 73,264-225,019	IGHG1, IGH, 13 more genes
nsv4374972	copy number variation	8	nstd173	human	GRCh37 chr19: 24,378,767-24,419,660 , GRCh38.p12 chr19: 24,195,965-24,236,858	0
nsv4376368	copy number variation	168	nstd173	human	GRCh37 chr6: 67,009,023-67,048,629 , GRCh38.p12 chr6: 66,299,130-66,338,736	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
nsv4387575	copy number variation	1	nstd173	human	GRCh37 chr12: 11,185,547-11,236,823 , GRCh38.p12 chr12: 11,032,948-11,084,224 , GRCh38.p12 chr12\|NT_187658.1: 231,953-285,343 , GRCh38.p12 chr12\|NW_003571050.1: 231,654-282,930	TAS2R64P, TAS2R68P, 5 more genes
nsv4380397	copy number variation	9	nstd173	human	GRCh37 chr14: 22,457,091-22,978,516 , GRCh38.p12 chr14: 21,988,851-22,509,533	TRD, TRAV22, 76 more genes
nsv4369094	copy number variation	1	nstd173	human	GRCh37 chrX: 28,117,236-28,389,716 , GRCh38.p12 chrX: 28,099,119-28,371,599	0
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
nsv4386412	copy number variation	21	nstd173	human	GRCh37 chr7: 38,293,950-38,382,540 , GRCh38.p12 chr7: 38,254,349-38,342,939	TRG, TRGJ1, 16 more genes
nsv4375229	copy number variation	71	nstd173	human	GRCh37 chr2: 34,701,643-34,723,190 , GRCh38.p12 chr2: 34,476,576-34,498,123	0

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Number of Variants: 20

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