dbVar for Gene (Select 155) - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv5200364	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633	LOC100130612, XPO7, 770 more genes
nsv4768211	inversion	1	nstd199	human		GRCh37 chr8: 23,474,464-53,327,098 , GRCh38.p12 chr8: 23,616,951-52,414,538	, ADRA1A, 411 more genes
nsv4756879	inversion	1	nstd199	human		GRCh37 chr8: 23,474,453-53,323,933 , GRCh38.p12 chr8: 23,616,940-52,411,373	, ADRA1A, 411 more genes
nsv4456811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385	TERF1, LOC107986945, 1511 more genes
nsv4456199	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 36,094,421-43,822,214 , GRCh38.p12 chr8: 36,236,903-43,967,071	AFG3L2P1, BRF2, 136 more genes
nsv4436744	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 36,486,830-37,992,515 , GRCh38.p12 chr8: 36,629,312-38,134,997	LOC105379380, LOC728024, 29 more genes
nsv4407203	copy number variation	1	nstd174	human		GRCh37 chr8: 37,821,486-37,825,374 , GRCh38.p12 chr8: 37,963,968-37,967,856	ADRB3
nsv4374467	copy number variation	1	nstd173	human		GRCh37 chr8: 37,692,087-37,883,453 , GRCh38.p12 chr8: 37,834,569-38,025,935	BRF2, RAB11FIP1, 4 more genes
nsv4349554	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385	LOC101929488, TEX15, 2105 more genes
nsv3923517	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 36,556,779-60,694,111 , GRCh37 chr8: 36,437,621-60,531,557 , GRCh38 chr8: 36,580,103-59,618,998	LOC105379380, TPT1P8, 320 more genes
nsv3923310	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098	LOC112268023, RPL23AP96, 2105 more genes
nsv3922311	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 37,428,611-47,058,107 , GRCh37.p13 chr8: 37,309,453-46,938,942 , GRCh38.p12 chr8: 37,451,935-46,027,320	CHRNB3, LOC105379380, 120 more genes
nsv3921773	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 12,511,855-43,310,472 , GRCh38 chr8: 12,609,975-43,336,172 , GRCh37 chr8: 12,467,484-43,191,315	RPL5P22, ZMAT4, 481 more genes
nsv3921545	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 33,964,607-47,058,107 , GRCh37.p13 chr8: 33,845,065-46,938,942 , GRCh38.p12 chr8: 33,987,547-46,027,320	SFRP1, DKK4, 148 more genes
nsv3921539	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 153,682-47,058,107 , GRCh37.p13 chr8: 163,682-46,938,942 , GRCh38.p12 chr8: 213,682-46,027,320	HSPD1P3, RNA5SP253, 770 more genes
nsv3921035	copy number variation	2	nstd102	human	Pathogenic	GRCh38 chr8: 12,728,904-43,673,207 , GRCh37 chr8: 12,586,413-43,528,350 , NCBI36 chr8: 12,630,784-43,647,507	MIR4287, RNU6-533P, 477 more genes
nsv3920952	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 176,452-37,879,246 , GRCh38 chr8: 226,452-38,021,728 , NCBI36 chr8: 166,452-37,998,403	MTUS1, LINC00208, 666 more genes
nsv3919926	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 12,490,999-40,543,052 , GRCh38 chr8: 12,633,490-40,685,533 , NCBI36 chr8: 12,535,370-40,662,209	SH2D4A, BMP1, 423 more genes
nsv3919419	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 34,169,768-43,014,044 , GRCh38 chr8: 34,312,250-43,158,901 , NCBI36 chr8: 34,289,310-43,133,201	PLEKHA2, STAR, 135 more genes
nsv3919317	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 6,986,629-38,672,221 , GRCh38 chr8: 7,141,697-38,695,546 , GRCh37 chr8: 6,999,219-38,553,064	LOC105379378, MRPS18CP2, 598 more genes

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Number of Variants: 20

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Items: 1 to 20 of 154

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Number of Variants: 20

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