15-1119-004 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
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
nsv4385917	copy number variation	155	nstd173	human	GRCh37 chr2: 98,138,417-98,162,188 , GRCh38.p12 chr2: 97,521,954-97,545,725	ANKRD36B
nsv4373295	copy number variation	124	nstd173	human	GRCh37 chr13: 69,248,299-69,268,719 , GRCh38.p12 chr13: 68,674,167-68,694,587	RN7SL761P
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
nsv4374395	copy number variation	2	nstd173	human	GRCh37 chr19: 55,297,882-55,347,661 , GRCh38.p12 chr19\|NT_187693.1: 768,996-818,775	KIR3DP1, KIR3DL1, 2 more genes
nsv4385108	copy number variation	8	nstd173	human	GRCh37 chrX: 1,460,449-1,506,403 , GRCh38.p12 chrX: 1,341,556-1,387,510	LOC101928032, , 2 more genes
nsv4384620	copy number variation	51	nstd173	human	GRCh37 chr6: 257,049-294,826 , GRCh38.p12 chr6: 257,049-294,826	DUSP22, , 1 more genes
nsv4372314	copy number variation	3	nstd173	human	GRCh37 chr1: 164,232,946-164,488,457 , GRCh38.p12 chr1: 164,263,709-164,519,220	RNU5F-6P, NMNAT1P2, 1 more genes
nsv4366564	copy number variation	6	nstd173	human	GRCh37 chr11: 58,810,465-58,855,182 , GRCh38.p12 chr11: 59,042,992-59,087,709	GLYATL1P4, LOC283194, 2 more genes
nsv4375167	copy number variation	2	nstd173	human	GRCh37 chr16: 33,863,684-34,012,167 , GRCh38.p12 chr16: 34,061,217-34,209,700	LOC348210, LINC00273, 7 more genes
nsv4365451	copy number variation	1	nstd173	human	GRCh37 chr14: 106,223,587-106,727,456 , GRCh38.p12 chr14: 105,786,368-106,270,859 , GRCh38.p12 chr14\|NT_187600.1: 225,019-1,214,078	IGHV3-47, IGHVII-40-1, 169 more genes
nsv4386873	copy number variation	3	nstd173	human	GRCh37 chr3: 12,737,141-12,766,343 , GRCh38.p12 chr3: 12,695,642-12,724,844	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
nsv4378146	copy number variation	18	nstd173	human	GRCh37 chr2: 78,701,691-78,721,998 , GRCh38.p12 chr2: 78,474,565-78,494,872	0
nsv4381750	copy number variation	2	nstd173	human	GRCh37 chr16: 32,038,694-33,765,646 , GRCh38.p12 chr16: 32,027,373-33,963,179	LOC105369183, BMS1P8, 59 more genes
nsv4384991	copy number variation	1	nstd173	human	GRCh37 chr14: 22,450,156-22,995,788 , GRCh38.p12 chr14: 21,981,915-22,526,820	TRAV19, TRAV40, 91 more genes
nsv4381583	copy number variation	9	nstd173	human	GRCh37 chr2: 110,873,835-111,365,996 , GRCh38.p12 chr2: 110,116,258-110,608,419	LOC102724875, LOC442041, 16 more genes
nsv4369089	copy number variation	21	nstd173	human	GRCh37 chr7: 38,286,527-38,409,689 , GRCh38.p12 chr7: 38,246,926-38,370,088	LOC103689914, TRGVA, 24 more genes
nsv4388033	copy number variation	1	nstd173	human	GRCh37 chr13: 65,642,515-65,742,850 , GRCh38.p12 chr13: 65,068,383-65,168,718	0
nsv4387566	copy number variation	315	nstd173	human	GRCh37 chr2: 34,701,655-34,727,784 , GRCh38.p12 chr2: 34,476,588-34,502,717	0

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Number of Variants: 20

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