lcmt2[All Fields] AND 1[has_clinical] - 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
nsv3901639	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 43,622,105-43,627,855 , GRCh38.p12 chr15: 43,329,907-43,335,657	LCMT2, ADAL
nsv3916249	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189	LCMT2, H3P40, 1616 more genes
nsv3919468	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189	LCMT2, RNU6-18P, 1442 more genes
nsv3903255	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 41,689,327-52,446,981 , GRCh38.p12 chr15: 41,397,129-52,154,784	LCMT2, RN7SKP101, 234 more genes
nsv3902367	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 42,850,434-49,592,633 , GRCh38.p12 chr15: 42,558,236-49,300,436	LCMT2, SERF2-C15ORF63, 142 more genes
nsv3924334	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr15: 42,785,627-43,342,260 , GRCh37 chr15: 43,077,825-43,634,458 , NCBI36 chr15: 40,865,117-41,421,750	LCMT2, KRT8P50, 13 more genes
nsv3900281	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 20,016,811-102,493,540 , GRCh38.p12 chr15: 19,811,558-101,953,337	LCMT2, MYZAP, 1750 more genes
nsv3913581	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 18,323,354-100,338,915 , GRCh37.p13 chr15: 20,063,340-102,521,392 , GRCh38.p12 chr15: 19,858,087-101,981,189	LCMT2, MIR4513, 1754 more genes
nsv3904086	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 20,071,673-102,461,162 , GRCh38.p12 chr15: 19,866,420-101,920,959	LCMT2, TMEM202, 1747 more genes
nsv3905138	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 20,733,395-102,511,616 , GRCh38.p12 chr15: 20,528,156-101,971,413	LCMT2, FES, 1738 more genes
nsv3892955	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr15: 22,770,422-102,429,112 , GRCh38.p12 chr15: 23,319,714-101,888,909	LCMT2, FAM81A, 1614 more genes
nsv3876912	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 31,115,047-102,354,857 , GRCh38.p12 chr15: 30,822,844-101,814,654	LCMT2, RNU6-953P, 1385 more genes
nsv3899559	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 41,745,084-102,354,798 , GRCh38.p12 chr15: 41,452,886-101,814,595	LCMT2, CILP, 1176 more genes
nsv3915997	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr15: 40,646,251-41,926,596 , GRCh37 chr15: 42,858,959-44,139,304 , GRCh38 chr15: 42,566,761-43,847,106	LCMT2, CKMT1B, 46 more genes
nsv4729554	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr15: 43,135,272-43,744,542 , GRCh38.p12 chr15: 42,843,074-43,452,344	LCMT2, EPB42, 16 more genes
nsv3918156	copy number variation	1	nstd102	human	Benign	NCBI36 chr15: 41,378,408-41,638,434 , GRCh37 chr15: 43,591,116-43,851,142 , GRCh38 chr15: 43,298,918-43,558,944	LCMT2, TUBGCP4, 7 more genes
nsv3918770	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr15: 20,280,728-100,338,915 , GRCh37.p13 chr15: 22,729,364-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189	LCMT2, SNRPCP18, 1622 more genes
nsv3918644	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr15: 20,313,935-100,338,915 , GRCh37.p13 chr15: 22,762,571-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189	LCMT2, SNORD116-23, 1622 more genes
nsv6291560	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 43,215,243-44,632,384 , GRCh38.p12 chr15: 42,923,045-44,340,186	LCMT2, PPIP5K1P1-CATSPER2, 44 more genes
nsv4457111	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 43,062,580-43,744,411 , GRCh38.p12 chr15: 42,770,382-43,452,213	LCMT2, CCNDBP1, 17 more genes

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 30

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Number of Variants: 20

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Supplemental Content

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Search details

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