dbVar for Gene (Select 84933) - 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
nsv5486310	copy number variation	1	nstd206	human		GRCh38 chr8: 123,213,745-123,218,556 , GRCh37.p13 chr8: 124,225,985-124,230,796	MIR4663, C8orf76
nsv5060033	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 121,938,227-125,485,728 , GRCh38.p12 chr8: 120,925,987-124,473,487	RNU6-756P, FAM83A, 53 more genes
nsv5035989	inversion	1	nstd200	human		GRCh38 chr8: 74,949,087-131,777,713 , GRCh37.p13 chr8: 75,861,322-132,789,960	, MIR7705, 715 more genes
nsv4675273	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 121,042,467-146,295,771 , GRCh38.p12 chr8: 120,030,228-145,070,385	TOP1MT, SLA, 379 more genes
nsv4457220	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 123,074,293-131,113,892 , GRCh38.p12 chr8: 122,062,054-130,101,646	ZHX1-C8orf76, SMILR, 117 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
nsv4456783	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 122,193,546-146,295,771 , GRCh38.p12 chr8: 121,181,306-145,070,385	HAS2, ZNF696, 369 more genes
nsv4455511	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 124,120,772-135,265,846 , GRCh38.p12 chr8: 123,108,532-134,253,603	MTSS1, PCAT2, 148 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
nsv4318515	inversion	1	nstd166	human		GRCh37.p13 chr8: 75,861,320-132,789,960 , GRCh38.p12 chr8: 74,949,085-131,777,713	, ANXA13, 716 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
nsv3921126	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 122,454,392-128,513,076 , GRCh37 chr8: 123,466,631-129,525,322 , NCBI36 chr8: 123,535,812-129,594,504	DERL1, RNU6-442P, 101 more genes
nsv3920738	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 113,580,402-145,054,634 , NCBI36 chr8: 114,661,807-146,250,824 , GRCh37 chr8: 114,592,631-146,280,020	KHDRBS3, DENND3-AS1, 438 more genes
nsv3919841	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 78,614,077-145,054,634 , GRCh37 chr8: 79,526,312-146,280,020 , NCBI36 chr8: 79,688,867-146,250,824	LY6S-AS1, LOC107984017, 911 more genes
nsv3919636	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 101,948,747-146,266,575 , GRCh38 chr8: 100,867,343-145,070,385 , GRCh37 chr8: 101,879,571-146,295,771	RSPO2, MTND2P35, 592 more genes
nsv3919282	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 191,530-146,280,020 , GRCh38 chr8: 241,530-145,054,634 , NCBI36 chr8: 181,530-146,250,824	MIR4662B, LOC101927845, 2104 more genes
nsv3919200	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 241,530-145,049,449 , GRCh37 chr8: 191,530-146,274,835 , NCBI36 chr8: 181,530-146,245,639	LOC112268023, LOC105375925, 2103 more genes
nsv3919183	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 123,763,846-124,373,809 , NCBI36 chr8: 123,833,027-124,442,990 , GRCh38 chr8: 122,751,607-123,361,569	FAM83A-AS1, TRM-CAT1-1, 20 more genes
nsv3916978	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 86,300,584-137,022,587 , NCBI36 chr8: 87,381,929-138,104,012 , GRCh37 chr8: 87,312,813-138,034,830	MIR5194, TRS-AGA2-5, 601 more genes
nsv3916777	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-146,295,771 , GRCh38 chr8: 208,048-145,070,385 , NCBI36 chr8: 148,048-146,266,575	RPL5P22, ARHGEF10, 2105 more genes

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Number of Variants: 20

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Organism

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 218

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Number of Variants: 20

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