dbVar for Gene (Select 137209) - 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
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
nsv4679444	copy number variation	1	nstd189	human		GRCh37.p13 chr8: 125,927,352-126,453,448 , GRCh38.p12 chr8: 124,915,110-125,441,206	SQLE, WASHC5, 8 more genes
nsv4675757	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 125,584,474-126,043,912 , GRCh38.p12 chr8: 124,572,233-125,031,670	LOC105375742, SQLE, 11 more genes
nsv4675718	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 124,878,368-126,737,708 , GRCh38.p12 chr8: 123,866,128-125,725,464	FER1L6-AS1, SQLE-DT, 30 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
nsv4607134	copy number variation	1	nstd183	human		GRCh37 chr8: 125,898,257-126,437,457 , GRCh38.p12 chr8: 124,886,015-125,425,215	SQLE, WASHC5, 7 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
nsv4456997	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 125,496,223-146,295,771 , GRCh38.p12 chr8: 124,483,982-145,070,385	LOC107986906, GPIHBP1, 317 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
nsv4455277	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 125,310,755-125,983,817 , GRCh38.p12 chr8: 124,298,514-124,971,575	LINC00964, MIR6844, 16 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

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Number of Variants: 20

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Items: 1 to 20 of 189

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Number of Variants: 20

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