dbVar for Gene (Select 100126343) - 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
nsv5381777	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 136,409,875-137,739,167 , GRCh38.p12 chr5: 137,074,186-138,403,478	HNRNPA0, SPOCK1, 24 more genes
nsv5381510	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 136,633,338-140,998,481 , GRCh38.p12 chr5: 137,297,649-141,618,914	RNA5SP195, LOC112267855, 174 more genes
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
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
nsv4945114	copy number variation	1	nstd200	human		GRCh38 chr5: 137,474,530-137,648,691 , GRCh37.p13 chr5: 136,810,219-136,984,380	MIR874, KLHL3, 1 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
nsv4455657	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 136,952,945-137,024,689 , GRCh38.p12 chr5: 137,617,256-137,689,000	KLHL3, MIR874
nsv4455440	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 136,810,103-136,982,225 , GRCh38.p12 chr5: 137,474,414-137,646,536	SPOCK1, KLHL3, 1 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
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
nsv3919979	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 132,737,257-137,772,727 , GRCh38 chr5: 133,401,565-138,437,038 , NCBI36 chr5: 132,765,156-137,800,626	FBXL21P, MIR5692C1, 92 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
nsv3910250	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 135,297,294-140,106,003 , GRCh37 chr5: 134,632,984-139,485,588 , NCBI36 chr5: 134,660,883-139,465,772	SNORD63, HSPA9, 94 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
nsv3886374	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028	LOC105374618, HARS1, 2499 more genes
nsv3884357	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr5: 86,400,000-154,000,000 , GRCh38.p12 chr5: 87,104,183-154,620,440	TXNDC15, PCDHAC1, 962 more genes
nsv3884275	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr5: 94,844,077-178,830,410 , GRCh38.p12 chr5: 95,508,373-179,403,409	LOC107986368, PRELID3BP9, 1258 more genes

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Number of Variants: 20

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Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Subject Phenotype Status

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Items: 1 to 20 of 73

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Number of Variants: 20

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