dbVar for Gene (Select 80167) - 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
nsv7148248	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr4: 127,964,562-127,965,767 , GRCh37.p13 chr4: 128,885,717-128,886,922	ABHD18, MFSD8
nsv7148159	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 127,949,707-127,984,521 , GRCh37.p13 chr4: 128,870,862-128,905,676	MFSD8, ABHD18
nsv7097233	copy number variation	2	nstd102	human	Pathogenic, Uncertain significance	GRCh37 chr4: 128,886,207-128,886,288 , GRCh38.p12 chr4: 127,965,052-127,965,133	ABHD18, MFSD8
nsv7097232	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 128,878,636-128,886,288 , GRCh38.p12 chr4: 127,957,481-127,965,133	ABHD18, MFSD8
nsv7096832	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 128,851,818-128,886,288 , GRCh38.p12 chr4: 127,930,663-127,965,133	MFSD8, ABHD18
nsv7096831	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 128,802,290-128,886,288 , GRCh38.p12 chr4: 127,881,135-127,965,133	RNU6-583P, ABHD18, 2 more genes
nsv7096819	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr4: 128,878,748-128,887,140 , GRCh38.p12 chr4: 127,957,593-127,965,985	ABHD18, MFSD8
nsv7096723	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 128,841,775-128,886,298 , GRCh38.p12 chr4: 127,920,620-127,965,143	ABHD18, MFSD8
nsv7052737	inversion	1	nstd229	human		GRCh38 chr4: 124,487,719-129,666,522 , GRCh37.p13 chr4: 125,408,874-130,587,677	H3P15, ANKRD50, 36 more genes
nsv7050150	inversion	1	nstd229	human		GRCh38 chr4: 127,983,622-128,091,755 , GRCh37.p13 chr4: 128,904,777-129,012,910	LARP1B, ABHD18, 1 more genes
nsv7043630	inversion	1	nstd229	human		GRCh38 chr4: 127,283,753-130,065,798 , GRCh37.p13 chr4: 128,204,908-130,986,953	SCLT1, JADE1, 30 more genes
nsv6757967	copy number variation	1	nstd229	human		GRCh38 chr4: 128,006,750-128,008,506 , GRCh37.p13 chr4: 128,927,905-128,929,661	ABHD18
nsv6757249	copy number variation	1	nstd229	human		GRCh38 chr4: 127,861,201-128,223,200 , GRCh37.p13 chr4: 128,782,356-129,144,355	FOSL1P1, ABHD18, 5 more genes
nsv6756531	copy number variation	1	nstd229	human		GRCh38 chr4: 127,959,501-128,157,000 , GRCh37.p13 chr4: 128,880,656-129,078,155	RPL15P8, MFSD8, 3 more genes
nsv6754865	copy number variation	1	nstd229	human		GRCh38 chr4: 127,922,418-128,006,708 , GRCh37.p13 chr4: 128,843,573-128,927,863	MFSD8, ABHD18
nsv6754374	copy number variation	1	nstd229	human		GRCh38 chr4: 127,968,385-128,004,059 , GRCh37.p13 chr4: 128,889,540-128,925,214	ABHD18
nsv6753821	copy number variation	1	nstd229	human		GRCh38 chr4: 127,882,340-128,230,605 , GRCh37.p13 chr4: 128,803,495-129,151,760	FOSL1P1, PLK4, 5 more genes
nsv6751489	copy number variation	1	nstd229	human		GRCh38 chr4: 128,021,641-128,021,711 , GRCh37.p13 chr4: 128,942,796-128,942,866	ABHD18
nsv6748967	copy number variation	1	nstd229	human		GRCh38 chr4: 127,982,301-128,107,900 , GRCh37.p13 chr4: 128,903,456-129,029,055	RPL15P8, LARP1B, 1 more genes
nsv6747929	copy number variation	1	nstd229	human		GRCh38 chr4: 128,020,701-128,106,400 , GRCh37.p13 chr4: 128,941,856-129,027,555	LARP1B, ABHD18, 1 more genes

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Number of Variants: 20

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Object Type

Organism

Variant Type

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Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Study Type

Subject Phenotype Status

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Items: 1 to 20 of 424

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Number of Variants: 20

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