dbVar for Gene (Select 64857) - 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
nsv5944000	copy number variation	1	nstd209	human		GRCh38 chr19: 39,387,653-39,412,021 , GRCh37.p13 chr19: 39,878,293-39,902,661	ZFP36, PAF1, 5 more genes
nsv5662764	insertion	1	nstd207	human		GRCh38 chr19: 39,413,589-39,413,589 , GRCh37.p13 chr19: 39,904,229-39,904,229	PLEKHG2
nsv5528258	copy number variation	1	nstd206	human		GRCh38 chr19: 39,409,499-39,412,022 , GRCh37.p13 chr19: 39,900,139-39,902,662	PLEKHG2, ZFP36, 2 more genes
nsv4632480	copy number variation	2	nstd183	human		GRCh37 chr19: 39,904,419-39,904,463 , GRCh38.p12 chr19: 39,413,779-39,413,823	PLEKHG2
nsv4624865	copy number variation	1	nstd183	human		GRCh37 chr19: 39,881,236-39,904,463 , GRCh38.p12 chr19: 39,390,596-39,413,823	ZFP36, PAF1, 5 more genes
nsv4457372	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575	ZNF461, LOC101927572, 735 more genes
nsv4257080	copy number variation	1	nstd166	human		GRCh37.p13 chr19: 39,918,698-39,922,161 , GRCh38.p12 chr19: 39,428,058-39,431,521	RPS16, PLEKHG2
nsv3913730	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354	BCKDHA, ADGRE5, 1102 more genes
nsv3912447	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 42,502,119-47,934,680 , GRCh37 chr19: 37,810,279-43,242,840 , GRCh38 chr19: 37,319,377-42,738,688	MIR8077, TRI-TAT1-1, 233 more genes
nsv3904885	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923	ZNF321P, ZNF861P, 2443 more genes
nsv3903203	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793	BABAM1, BEST2, 2426 more genes
nsv3903092	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521	LENG8, SYDE1, 2408 more genes
nsv3895066	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 37,582,250-41,630,908 , GRCh38.p12 chr19: 37,091,348-41,125,003	RNU6-140P, COQ8B, 162 more genes
nsv3890776	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 39,888,449-39,903,088 , GRCh38.p12 chr19: 39,397,809-39,412,448	MIR4530, ZFP36, 3 more genes
nsv3169031	copy number variation	1	nstd158	human		GRCh38.p12 chr19: 38,412,977-41,901,266 , GRCh37 chr19: 38,903,617-42,405,416	, ACTN4, 162 more genes
nsv3168446	copy number variation	1	nstd158	human		GRCh37 chr19: 35,445,908-45,506,757 , GRCh38.p12 chr19: 34,955,004-45,003,499	, ACTN4, 449 more genes
nsv3167054	copy number variation	1	nstd151	human		GRCh37 chr19: 39,909,371-39,909,648 , GRCh38.p12 chr19: 39,418,731-39,419,008	PLEKHG2
nsv3166670	copy number variation	1	nstd151	human		GRCh37 chr19: 39,909,371-39,911,641 , GRCh38.p12 chr19: 39,418,731-39,421,001	PLEKHG2
nsv3159968	copy number variation	1	nstd151	human		GRCh37 chr19: 39,911,263-39,916,022 , GRCh38.p12 chr19: 39,420,623-39,425,382	PLEKHG2
nsv3159836	copy number variation	2	nstd151	human		GRCh37 chr19: 39,906,985-39,909,648 , GRCh38.p12 chr19: 39,416,345-39,419,008	PLEKHG2

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 147

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Number of Variants: 20

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