dbVar for Gene (Select 3810) - dbVar - NCBI

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Items: 5

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Number of Variants: 5

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4536394	copy number variation	1	nstd166	human		GRCh37.p13 chr19: 55,054,999-55,564,000 , GRCh38.p12 chr19\|NW_003571059.2: 705,634-970,997 , GRCh38.p12 chr19\|NW_003571055.2: 399,097-697,834 , GRCh38.p12 chr19\|NT_187693.1: 526,113-894,467 , GRCh38.p12 chr19\|NW_003571061.2: 363,080-764,793 , GRCh38.p12 chr19\|NW_003571060.1: 448,507-955,414 , GRCh38.p12 chr19\|NT_187675.1: 4-282,224 , GRCh38.p12 chr19\|NW_016107303.1: 1-293,522 , GRCh38.p12 chr19: 54,543,790-54,911,985 , GRCh38.p12 chr19\|NW_003571054.1: 449,989-956,030	, LILRA2, 45 more genes
nsv3899237	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 55,017,416-55,602,115 , GRCh38.p12 chr19\|NW_003571060.1: 410,918-987,100 , GRCh38.p12 chr19\|NW_016107303.1: 1-293,522 , GRCh38.p12 chr19\|NW_003571061.2: 363,080-796,479 , GRCh38.p12 chr19\|NW_003571055.2: 399,097-729,520 , GRCh38.p12 chr19\|NW_003571054.1: 412,407-987,716 , GRCh38.p12 chr19: 54,506,200-54,911,985 , GRCh38.p12 chr19\|NT_187693.1: 488,530-894,467 , GRCh38.p12 chr19\|NW_003571059.2: 705,634-1,002,683	NLRP7, KIR3DP1, 46 more genes
nsv2755100	copy number variation	1	nstd130	human		NCBI36 chr19: 59,654,186-60,141,567 , GRCh37.p13 chr19\|NW_004166865.1: 667,012-912,755 , GRCh38.p12 chr19: 54,451,197-54,911,985 , GRCh38.p12 chr19\|NT_187693.1: 433,488-894,467 , GRCh38.p12 chr19\|NW_003571061.2: 363,080-650,548 , GRCh38.p12 chr19\|NW_003571060.1: 355,882-842,739 , GRCh38.p12 chr19\|NW_003571054.1: 357,709-841,785 , GRCh38.p12 chr19\|NT_187636.1: 3-248,807 , GRCh38.p12 chr19\|NT_187675.1: 4-282,224 , GRCh38.p12 chr19\|NW_016107303.1: 1-293,522	NLRP7, LAIR2, 44 more genes
nsv2750201	copy number variation	2	nstd130	human		NCBI36 chr19: 59,654,186-60,143,609 , GRCh37.p13 chr19\|NW_004166865.1: 667,012-914,797 , GRCh38.p12 chr19: 54,451,197-54,911,985 , GRCh38.p12 chr19\|NT_187693.1: 433,488-894,467 , GRCh38.p12 chr19\|NW_003571061.2: 363,080-652,590 , GRCh38.p12 chr19\|NW_003571060.1: 355,882-844,781 , GRCh38.p12 chr19\|NW_003571054.1: 357,709-843,827 , GRCh38.p12 chr19\|NT_187636.1: 3-248,807 , GRCh38.p12 chr19\|NT_187675.1: 4-282,224 , GRCh38.p12 chr19\|NW_016107303.1: 1-293,522	KIR2DP1, KIR2DL4, 44 more genes
nsv1194440	copy number variation	2	nstd113	human		NCBI36 chr19: 59,654,889-60,141,416 , GRCh37.p13 chr19\|NW_004166865.1: 667,012-912,604 , GRCh38.p12 chr19: 54,451,900-54,911,985 , GRCh38.p12 chr19\|NT_187693.1: 434,191-894,467 , GRCh38.p12 chr19\|NW_003571061.2: 363,080-650,397 , GRCh38.p12 chr19\|NW_003571060.1: 356,585-842,588 , GRCh38.p12 chr19\|NW_003571054.1: 358,412-841,634 , GRCh38.p12 chr19\|NT_187636.1: 3-248,807 , GRCh38.p12 chr19\|NT_187675.1: 4-282,224 , GRCh38.p12 chr19\|NW_016107303.1: 1-293,522	KIR2DL2, KIR2DS5, 44 more genes

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