dbVar for Gene (Select 134549) - 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
nsv5458850	copy number variation	1	nstd206	human		GRCh38 chr5: 132,826,197-132,826,494 , GRCh37.p13 chr5: 132,161,889-132,162,186	SHROOM1
nsv5036421	inversion	1	nstd200	human		GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836	, PRR16, 1116 more genes
nsv5034346	inversion	1	nstd200	human		GRCh38 chr5: 99,223,339-135,778,784 , GRCh37.p13 chr5: 98,559,043-135,114,473	, NUDT12, 438 more genes
nsv4947215	copy number variation	1	nstd200	human		GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636	, TGFBI, 937 more genes
nsv4885569	inversion	1	nstd200	human		GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835	, UBE2B, 1116 more genes
nsv4872282	inversion	1	nstd200	human		GRCh37 chr5: 98,106,197-132,803,784 , GRCh38.p12 chr5: 98,770,493-133,468,092	, LEAP2, 395 more genes
nsv4436202	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379	RNU1-150P, RNU6-727P, 1757 more genes
nsv4320566	inversion	1	nstd166	human		GRCh37.p13 chr5: 114,283,102-148,759,757 , GRCh38.p12 chr5: 114,947,405-149,380,194	, ACTBP4, 606 more genes
nsv4129463	copy number variation	1	nstd166	human		GRCh37.p13 chr5: 132,161,889-132,162,186 , GRCh38.p12 chr5: 132,826,197-132,826,494	SHROOM1
nsv3971975	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr5: 126,377,719-136,270,989 , GRCh38.p12 chr5: 127,042,027-136,935,300	ACTBP4, CAMLG, 157 more genes
nsv3923830	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 132,151,895-134,718,848 , GRCh38 chr5: 132,816,203-135,383,158 , NCBI36 chr5: 132,179,794-134,746,747	MTND5P11, TCF7, 60 more genes
nsv3923414	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 130,196,621-154,701,371 , NCBI36 chr5: 130,224,520-154,681,564 , GRCh38 chr5: 130,860,928-155,321,811	HNRNPA3P7, RNU6-456P, 514 more genes
nsv3920627	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 126,864,591-135,314,282 , GRCh37.p13 chr5: 126,836,692-135,286,383 , GRCh38.p12 chr5: 127,501,000-135,950,694	MIR1289-2, DCANP1, 138 more genes
nsv3916850	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 130,962,196-135,150,743 , NCBI36 chr5: 130,990,095-135,178,642 , GRCh38 chr5: 131,626,503-135,815,054	SLC25A48-AS1, CTB-3M24.3, 96 more genes
nsv3914009	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 129,211,386-152,713,299 , GRCh38 chr5: 129,847,794-153,353,546 , GRCh37 chr5: 129,183,487-152,733,106	UQCRQ, SNHG4, 489 more genes
nsv3912937	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 105,955,289-155,551,397 , NCBI36 chr5: 105,983,188-155,483,975 , GRCh38 chr5: 106,619,588-156,124,387	LINC01023, CTB-99A3.1, 783 more genes
nsv3912593	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr5: 332,389-180,837,866 , GRCh37.p13 chr5: 279,389-180,905,260 , GRCh38.p12 chr5: 279,274-181,478,259	LOC105378993, LOC107986375, 2492 more genes
nsv3911932	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 125,774,098-132,209,659 , NCBI36 chr5: 125,801,997-132,237,558 , GRCh38 chr5: 126,438,406-132,873,967	LOC105379176, GDF9, 93 more genes
nsv3889848	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719	MEGF10, LOC100128407, 2080 more genes
nsv3888061	copy number variation	1	nstd102	human	Benign	GRCh37 chr5: 132,150,484-132,161,784 , GRCh38.p12 chr5: 132,814,792-132,826,092	SOWAHA, SHROOM1

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Number of Variants: 20

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