dbVar for Gene (Select 26098) - 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
nsv6112765	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 118,247,181-135,435,319 , GRCh38.p12 chr10: 116,487,669-133,621,815	STK32C, LOC105378542, 266 more genes
nsv5980446	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 122,785,023-135,457,222 , GRCh38.p12 chr10: 121,025,510-133,643,718	LINC02641, CFAP46, 194 more genes
nsv5850509	copy number variation	1	nstd209	human		GRCh38 chr10: 125,715,251-125,717,733 , GRCh37.p13 chr10: 127,403,820-127,406,302	EDRF1-DT, EDRF1
nsv5722226	mobile element insertion	2	nstd211	human		GRCh38 chr10: 125,731,810-125,731,810 , GRCh37.p13 chr10: 127,420,379-127,420,379	EDRF1
nsv5636388	insertion	1	nstd207	human		GRCh38 chr10: 125,731,795-125,731,795 , GRCh37.p13 chr10: 127,420,364-127,420,364	EDRF1
nsv5590137	copy number variation	1	nstd207	human		GRCh38 chr10: 125,710,948-125,717,559 , GRCh37.p13 chr10: 127,399,517-127,406,128	EDRF1-DT, EDRF1
nsv5558528	mobile element insertion	1	nstd206	human		GRCh38 chr10: 125,731,810-125,731,861 , GRCh37.p13 chr10: 127,420,379-127,420,430	EDRF1
nsv5508376	copy number variation	1	nstd206	human		GRCh38 chr10: 125,710,950-125,717,560 , GRCh37.p13 chr10: 127,399,519-127,406,129	EDRF1-DT, EDRF1
nsv5315279	copy number variation	1	nstd204	human		GRCh37.p13 chr10: 127,399,509-127,406,138 , GRCh38.p13 chr10: 125,710,940-125,717,569	EDRF1, EDRF1-DT
nsv5196649	mobile element insertion	1	nstd203	human		GRCh38 chr10: 125,731,810-125,731,810 , GRCh37.p13 chr10: 127,420,379-127,420,379	EDRF1
nsv5191642	mobile element insertion	1	nstd203	human		GRCh38 chr10: 125,731,795-125,731,810 , GRCh37.p13 chr10: 127,420,364-127,420,379	EDRF1
nsv5137531	mobile element insertion	1	nstd203	human		GRCh38 chr10: 125,718,169-125,718,181 , GRCh37.p13 chr10: 127,406,738-127,406,750	EDRF1-DT, EDRF1
nsv5128819	mobile element insertion	1	nstd203	human		GRCh38 chr10: 125,723,815-125,723,815 , GRCh37.p13 chr10: 127,412,384-127,412,384	EDRF1
nsv4983971	copy number variation	1	nstd200	human		GRCh38 chr10: 125,039,754-126,334,238 , GRCh37.p13 chr10: 126,728,323-128,022,807	, ADAM12, 28 more genes
nsv4977431	copy number variation	1	nstd200	human		GRCh38 chr10: 125,744,858-125,745,100 , GRCh37.p13 chr10: 127,433,427-127,433,669	EDRF1, EDRF1-AS1
nsv4977430	copy number variation	1	nstd200	human		GRCh38 chr10: 125,710,950-125,717,560 , GRCh37.p13 chr10: 127,399,519-127,406,129	EDRF1-DT, EDRF1
nsv4848868	copy number variation	1	nstd200	human		GRCh37 chr10: 127,399,519-127,406,129 , GRCh38.p12 chr10: 125,710,950-125,717,560	EDRF1, EDRF1-DT
nsv4693623	mobile element insertion	2	nstd186	human		GRCh37 chr10: 127,420,364-127,420,364 , GRCh38.p12 chr10: 125,731,795-125,731,795	EDRF1
nsv4675991	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 119,996,339-135,427,143 , GRCh38.p12 chr10: 118,236,827-133,613,639	STK32C, LOC105378542, 237 more genes
nsv4613153	copy number variation	1	nstd183	human		GRCh37 chr10: 127,445,365-127,445,671 , GRCh38.p12 chr10: 125,756,796-125,757,102	EDRF1

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Number of Variants: 20

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Organism

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 223

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Number of Variants: 20

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