M2143 AND nstd157 - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
nsv3318245	copy number variation	1	nstd157	human	GRCh37 chr2: 144,883,863-144,897,218 , GRCh38.p12 chr2: 144,126,296-144,139,651	GTDC1
nsv3317630	copy number variation	1	nstd157	human	GRCh37 chr5: 17,639,913-17,651,582 , GRCh38.p12 chr5: 17,639,804-17,651,473	LOC391768
nsv3318516	copy number variation	22	nstd157	human	GRCh37 chr13: 64,225,427-64,236,288 , GRCh38.p12 chr13: 63,651,294-63,662,155	LOC105370236
nsv3318342	copy number variation	3	nstd157	human	GRCh37 chr2: 115,535,198-115,542,382 , GRCh38.p12 chr2: 114,777,621-114,784,805	DPP10
nsv3318029	copy number variation	27	nstd157	human	GRCh37 chr18: 41,976,831-41,982,102 , GRCh38.p12 chr18: 44,396,866-44,402,137	LINC01478
nsv3318976	copy number variation	1	nstd157	human	GRCh37 chr16: 29,684,788-29,692,414 , GRCh38.p12 chr16: 29,673,467-29,681,093	QPRT
nsv3318357	copy number variation	1	nstd157	human	GRCh37 chr5: 818,658-824,025 , GRCh38.p12 chr5: 818,543-823,910	ZDHHC11
nsv3318556	copy number variation	1	nstd157	human	GRCh38.p12 chr2: 218,636,605-218,647,012 , GRCh37 chr2: 219,501,328-219,511,735	ZNF142, PLCD4
nsv3317283	copy number variation	2	nstd157	human	GRCh37 chr17: 16,578,053-16,587,108 , GRCh38.p12 chr17: 16,674,739-16,683,794	CCDC144A, RNASEH1P2
nsv3317918	copy number variation	12	nstd157	human	GRCh38.p12 chr21: 43,402,991-43,417,949 , GRCh37 chr21: 44,822,871-44,837,829	SIK1,
nsv3318690	copy number variation	14	nstd157	human	GRCh38.p12 chr2: 38,733,349-38,744,481 , GRCh37 chr2: 38,960,491-38,971,623	SRSF7, GALM
nsv3318220	copy number variation	21	nstd157	human	GRCh38.p12 chr19: 20,418,529-20,532,427 , GRCh37 chr19: 20,601,335-20,715,233	ZNF826P, ZNF737, 3 more genes
nsv3318908	copy number variation	3	nstd157	human	GRCh37 chr2: 89,253,479-90,255,826 , GRCh38.p12 chr2: 88,953,960-90,216,960	ABCD1P1, IGKV6D-41, 74 more genes
nsv3318817	copy number variation	5	nstd157	human	GRCh37 chr9: 66,771,643-66,862,785 , GRCh38.p12 chr9: 40,818,615-40,909,757	0
nsv3318308	copy number variation	19	nstd157	human	GRCh37 chr16: 19,945,540-19,962,636 , GRCh38.p12 chr16: 19,934,218-19,951,314	0
nsv3318432	copy number variation	41	nstd157	human	GRCh37 chr8: 5,595,511-5,605,706 , GRCh38.p12 chr8: 5,737,989-5,748,184	0
nsv3318039	copy number variation	18	nstd157	human	GRCh37 chr13: 58,589,893-58,599,174 , GRCh38.p12 chr13: 58,015,759-58,025,040	0
nsv3317366	copy number variation	4	nstd157	human	GRCh37 chr2: 106,347,912-106,353,107 , GRCh38.p12 chr2: 105,731,455-105,736,650	0
nsv3318898	copy number variation	1	nstd157	human	GRCh38.p12 chr6: 27,667,148-27,687,785 , GRCh37 chr6: 27,634,927-27,655,564	TRI-AAT2-1, TRI-AAT8-1, 4 more genes
nsv3318671	copy number variation	17	nstd157	human	GRCh37 chr5: 180,176,005-180,195,526 , GRCh38.p12 chr5: 180,749,005-180,768,526	0

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Number of Variants: 20

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