sample354 AND nstd145 - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
nsv3115697	copy number variation	53	nstd145	human	GRCh37 chr11: 7,814,824-7,826,930 , GRCh38.p12 chr11: 7,793,277-7,805,383 , GRCh38.p12 chr11\|NT_187583.1: 14,145-26,251 , GRCh38.p12 chr11\|NW_011332695.1: 14,145-26,251	OR5P2
nsv3110942	copy number variation	60	nstd145	human	GRCh37 chr7: 91,033,585-91,042,496 , GRCh38.p12 chr7: 91,404,270-91,413,181	LINC02932
nsv3114178	copy number variation	107	nstd145	human	GRCh37 chr6: 53,928,991-53,933,879 , GRCh38.p12 chr6: 54,064,193-54,069,081	MLIP
nsv3115624	copy number variation	7	nstd145	human	GRCh37 chr15: 33,907,612-33,910,710 , GRCh38.p12 chr15: 33,615,411-33,618,509	RYR3
nsv3115311	copy number variation	23	nstd145	human	GRCh37 chr3: 189,737,302-189,740,185 , GRCh38.p12 chr3: 190,019,513-190,022,396	P3H2
nsv3111369	copy number variation	4	nstd145	human	GRCh37 chr2: 100,103,710-100,105,401 , GRCh38.p12 chr2: 99,487,248-99,488,939	REV1
nsv3117991	copy number variation	1	nstd145	human	GRCh37 chr2: 81,161,544-81,247,334 , GRCh38.p12 chr2: 80,934,420-81,020,210	LOC105374827
nsv3113370	copy number variation	2	nstd145	human	GRCh37 chr1: 152,556,183-152,586,200 , GRCh38.p12 chr1: 152,583,707-152,613,724	LCE3B, LCE3C
nsv3112813	copy number variation	50	nstd145	human	GRCh37 chr14: 35,606,293-35,613,839 , GRCh38.p12 chr14: 35,137,087-35,144,633	PRORP, RPL23AP70
nsv3112965	copy number variation	35	nstd145	human	GRCh37 chr1: 72,766,586-72,770,822 , GRCh38.p12 chr1: 72,300,903-72,305,139 , GRCh38.p12 chr1\|NW_018654707.1: 13,170-17,406	RPL31P12, LOC105378797
nsv3112361	copy number variation	13	nstd145	human	GRCh37 chr5: 180,374,509-180,429,599 , GRCh38.p12 chr5: 180,947,509-181,002,599	BTNL3, BTNL8, 3 more genes
nsv3110439	copy number variation	1	nstd145	human	GRCh37 chr17: 39,423,803-39,433,492 , GRCh38.p12 chr17: 41,267,551-41,277,240 , GRCh38.p12 chr17\|NW_003871093.1: 29,870-39,559	KRTAP9-11P, KRTAP9-7, 1 more genes
nsv3110903	copy number variation	122	nstd145	human	GRCh37 chr2: 52,749,700-52,784,734 , GRCh38.p12 chr2: 52,522,562-52,557,596	0
nsv3113406	copy number variation	69	nstd145	human	GRCh37 chr4: 10,211,362-10,234,173 , GRCh38.p12 chr4: 10,209,738-10,232,549	0
nsv3116118	copy number variation	124	nstd145	human	GRCh37 chr6: 103,737,578-103,760,261 , GRCh38.p12 chr6: 103,289,703-103,312,386	0
nsv3115389	copy number variation	117	nstd145	human	GRCh37 chr9: 23,363,340-23,377,598 , GRCh38.p12 chr9: 23,363,342-23,377,600	0
nsv3116294	copy number variation	23	nstd145	human	GRCh37 chr2: 146,863,450-146,876,325 , GRCh38.p12 chr2: 146,105,882-146,118,757	0
nsv3111842	copy number variation	1	nstd145	human	GRCh37 chr3: 86,333,801-86,338,772 , GRCh38.p12 chr3: 86,284,651-86,289,622	0
nsv3113095	copy number variation	21	nstd145	human	GRCh37 chr11: 107,784,308-107,788,398 , GRCh38.p12 chr11: 107,913,582-107,917,672	0
nsv3111610	copy number variation	35	nstd145	human	GRCh37 chr17: 52,160,322-52,162,909 , GRCh38.p12 chr17: 54,082,961-54,085,548	0

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Number of Variants: 20

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