lpcat4[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
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	LPCAT4, 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	LPCAT4, RNU6-18P, 1442 more genes
nsv3917652	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 20,249,886-36,169,075 , GRCh38 chr15: 23,319,714-38,089,582 , GRCh37 chr15: 22,698,522-38,381,783	LPCAT4, LOC105370764, 345 more genes
nsv4674936	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 22,770,421-36,861,479 , GRCh38.p12 chr15: 23,319,714-36,569,278	LPCAT4, SNORD115-48, 330 more genes
nsv3921026	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 22,830,109-35,283,797 , GRCh38 chr15: 25,033,869-37,204,304 , GRCh37 chr15: 25,279,016-37,496,505	LPCAT4, SNORD116-17, 303 more genes
nsv3908896	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 6,671,304-16,243,921 , GRCh38 chr2: 6,531,172-16,103,799 , NCBI36 chr2: 6,588,755-16,161,372	RNU6-1288P, MIR7515HG, 138 more genes
nsv3915967	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr15: 32,635,803-40,233,825 , GRCh37 chr15: 32,928,004-40,526,026 , NCBI36 chr15: 30,715,296-38,313,318	LPCAT4, ANP32AP1, 112 more genes
nsv3920384	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 30,405,629-37,473,561 , GRCh38 chr15: 32,326,136-39,394,068 , GRCh37 chr15: 32,618,337-39,686,269	LPCAT4, PGBD4, 113 more genes
nsv6315190	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 33,809,650-40,027,263 , GRCh38.p12 chr15: 33,517,449-39,735,062	LPCAT4, RYR3, 84 more genes
nsv4675391	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 34,197,488-38,656,254 , GRCh38.p12 chr15: 33,905,287-38,364,053	LPCAT4, TPST2P1, 65 more genes
nsv4675702	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 31,675,452-35,689,958 , GRCh38.p12 chr15: 31,383,249-35,397,757 , GRCh38.p12 chr15\|NT_187660.1: 2,721,316-5,161,414	LPCAT4, AVEN, 113 more genes
nsv7096918	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr2: 7,968,276-10,192,634 , GRCh38.p12 chr2: 7,828,145-10,052,507	ITGB1BP1, LINC00299, 37 more genes
nsv7094366	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 34,526,072-35,087,019 , GRCh38.p12 chr15: 34,233,871-34,794,818	LPCAT4, NUTM1, 16 more genes
nsv6315390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305	LOC112268439, RNA5SP116, 3737 more genes
nsv3874648	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305	IGKV2OR2-10, LOC105374848, 3737 more genes
nsv3885544	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609	RNU6-674P, KANSL3, 3735 more genes
nsv3882615	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232	MTND2P22, LOC112268410, 3724 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	LPCAT4, 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	LPCAT4, 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	LPCAT4, TMEM202, 1747 more genes

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Number of Variants: 20

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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 59

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Number of Variants: 20

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