SCOS_31 AND nstd53 - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
nsv870374	copy number variation	79	nstd53	human	NCBI36 chr1: 72,541,502-72,589,682 , GRCh38.p12 chr1: 72,303,231-72,351,411 , GRCh37.p13 chr1: 72,768,914-72,817,094 , GRCh38.p12 chr1\|NW_018654707.1: 15,498-72,636	LOC105378797
nsv870002	copy number variation	49	nstd53	human	NCBI36 chr17: 41,527,764-41,566,540 , GRCh37.p13 chr17: 44,176,718-44,210,763 , GRCh38.p12 chr17: 46,094,581-46,133,397 , GRCh38.p12 chr17\|NT_187663.1: 796,687-835,504 , GRCh37.p13 chr17\|NT_167251.1: 655,282-689,337 , GRCh38.p12 chr17\|NT_167251.2: 653,289-691,821	KANSL1
nsv870244	copy number variation	26	nstd53	human	NCBI36 chr7: 141,408,072-141,438,504 , GRCh37.p13 chr7: 141,761,603-141,792,035 , GRCh38.p12 chr7: 142,061,803-142,092,235 , GRCh38.p12 chr7\|NT_187562.1: 23,683-54,115 , GRCh37.p13 chr7\|NW_003571040.1: 203,754-234,186	MGAM
nsv869729	copy number variation	57	nstd53	human	NCBI36 chr1: 150,823,126-150,848,509 , GRCh38.p12 chr1: 152,584,026-152,609,409 , GRCh37.p13 chr1: 152,556,502-152,581,885	LCE3C
nsv870223	copy number variation	9	nstd53	human	GRCh38.p12 chr8: 39,445,296-39,465,166 , NCBI36 chr8: 39,421,972-39,441,842 , GRCh37.p13 chr8: 39,302,815-39,322,685	ADAM3A
nsv869663	copy number variation	9	nstd53	human	NCBI36 chr12: 31,223,524-31,237,505 , GRCh38.p12 chr12: 31,179,323-31,193,304 , GRCh37.p13 chr12: 31,332,257-31,346,238 , GRCh38.p12 chr12\|NT_187587.1: 70,117-84,098	OVOS2
nsv870424	copy number variation	2	nstd53	human	GRCh38.p12 chr6: 162,197,226-162,233,059 , NCBI36 chr6: 162,538,248-162,574,081 , GRCh37.p13 chr6: 162,618,258-162,654,091	PRKN, LOC105378097
nsv869730	copy number variation	122	nstd53	human	GRCh38.p12 chr8: 39,377,532-39,528,580 , NCBI36 chr8: 39,354,208-39,505,256 , GRCh37.p13 chr8: 39,235,051-39,386,099	ADAM3A, ADAM5
nsv870172	copy number variation	4	nstd53	human	NCBI36 chr16: 21,382,599-21,501,073 , GRCh38.p12 chr16: 21,463,777-21,582,251 , GRCh37.p13 chr16: 21,475,098-21,593,572	SLC7A5P2, LOC646828, 2 more genes
nsv869555	copy number variation	13	nstd53	human	NCBI36 chr14: 105,961,797-105,988,215 , GRCh38.p12 chr14: 106,434,842-106,461,245 , GRCh37.p13 chr14: 106,890,752-106,917,170 , GRCh38.p12 chr14\|NT_187600.1: 926,521-952,924 , GRCh37.p13 chr14\|NW_004166863.1: 1,098,009-1,124,412	IGH, IGHVII-40-1, 2 more genes
nsv869910	copy number variation	14	nstd53	human	GRCh38.p12 chr2: 241,914,496-242,092,126 , NCBI36 chr2: 242,505,320-242,682,950 , GRCh37.p13 chr2: 242,856,647-243,034,277 , GRCh38.p12 chr2\|NT_187647.1: 1-135,836 , GRCh38.p12 chr2\|NT_187523.1: 1-136,196	LOC285097, LINC01881, 4 more genes
nsv870009	copy number variation	36	nstd53	human	GRCh37.p13 chr3: 195,354,183-195,457,709 , GRCh38.p12 chr3: 195,627,312-195,730,838 , NCBI36 chr3: 196,835,472-196,943,380 , GRCh38.p12 chr3\|NT_187649.1: 63,861-139,787 , GRCh38.p12 chr3\|NT_187688.1: 63,861-140,349 , GRCh38.p12 chr3\|NT_187690.1: 63,868-141,061 , GRCh38.p12 chr3\|NT_187691.1: 64,038-142,498 , GRCh38.p12 chr3\|NT_187678.1: 65,206-143,431 , GRCh38.p12 chr3\|NT_187689.1: 23,110-101,335 , GRCh38.p12 chr3\|NT_187532.1: 23,110-101,335	MUC20, MIR570HG, 7 more genes
nsv869590	copy number variation	24	nstd53	human	NCBI36 chr15: 19,846,001-19,933,992 , GRCh38.p12 chr15: 22,056,686-22,144,677 , GRCh37.p13 chr15: 22,344,637-22,432,628	OR4H6P, OR4N4, 4 more genes
nsv870216	copy number variation	1	nstd53	human	GRCh38.p12 chr10: 45,662,767-47,923,579 , NCBI36 chr10: 45,478,221-47,021,415 , GRCh37.p13 chr10: 46,158,215-47,531,169 , GRCh37.p13 chr10\|NW_003871068.1: 1-2,010,264	CTSLP2, GDF2, 72 more genes
nsv870136	copy number variation	33	nstd53	human	NCBI36 chr15: 18,876,700-19,465,359 , GRCh38.p12 chr15: 20,411,433-21,498,353 , GRCh37.p13 chr15: 20,616,686-22,141,158	NBEAP1, IGHV1OR15-6, 44 more genes
nsv870032	copy number variation	7	nstd53	human	NCBI36 chrX: 16,054-85,768 , GRCh37.p13 chrX: 76,054-145,768 , GRCh38.p12 chrX: 26,054-229,101	0
nsv870413	copy number variation	41	nstd53	human	GRCh38.p12 chr2: 34,472,710-34,513,110 , NCBI36 chr2: 34,551,281-34,591,681 , GRCh37.p13 chr2: 34,697,777-34,738,177	0
nsv869977	copy number variation	2	nstd53	human	GRCh38.p12 chr22: 11,820,445-12,904,788 , NCBI36 chr1: 141,559,525-143,623,628 , GRCh37.p13 chr1: 142,618,002-144,912,271	LOC101928041, FRG1GP, 12 more genes
nsv870306	copy number variation	42	nstd53	human	NCBI36 chr16: 32,547,672-33,320,529 , GRCh38.p12 chr16: 32,628,850-33,610,561 , GRCh37.p13 chr16: 32,640,171-33,413,028 , GRCh37.p13 chr1\|NW_003871055.3: 103,116-1,641,917	TP53TG3, IGHV3OR16-15, 28 more genes
nsv869703	copy number variation	13	nstd53	human	NCBI36 chr16: 34,329,577-34,619,028 , GRCh38.p12 chr16: 35,237,705-35,527,156 , GRCh37.p13 chr16: 34,472,076-34,761,527	FRG2DP, LINC01566, 25 more genes

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Number of Variants: 20

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