dbVar for Gene (Select 151658) - 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
nsv5686860	mobile element insertion	1	nstd211	human		GRCh38 chr3: 107,877,090-107,877,090 , GRCh37.p13 chr3: 107,595,937-107,595,937	LINC00635
nsv5402407	mobile element insertion	1	nstd206	human		GRCh38 chr3: 107,877,090-107,877,141 , GRCh37.p13 chr3: 107,595,937-107,595,988	LINC00635
nsv5361842	translocation	1	nstd200	human		GRCh38 chr4: 82,001,433-82,001,433 , GRCh38 chr3: 107,850,619-107,850,619 , GRCh37.p13 chr4: 82,922,586-82,922,586 , GRCh37.p13 chr3: 107,569,466-107,569,466	LINC00635
nsv5093478	mobile element insertion	1	nstd203	human		GRCh38 chr3: 107,877,074-107,877,090 , GRCh37.p13 chr3: 107,595,921-107,595,937	LINC00635
nsv5036857	inversion	1	nstd200	human		GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646	, FBRSL1P1, 801 more genes
nsv4674254	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 101,812,245-112,174,485 , GRCh38.p12 chr3: 102,093,401-112,455,638	IFT57, LINC00636, 111 more genes
nsv4540600	insertion	1	nstd166	human		GRCh37.p13 chr3: 107,595,921-107,595,921 , GRCh38.p12 chr3: 107,877,074-107,877,074	LINC00635
nsv4436512	complex substitution	1	nstd102	human	association	GRCh37.p13 chr3: 107,043,012-108,401,146 , GRCh38.p12 chr3: 107,324,165-108,682,299 , NCBI36 chr3: 108,525,702-109,883,836	CD47, DZIP3, 16 more genes
nsv4317801	inversion	1	nstd166	human		GRCh37.p13 chr3: 106,160,269-123,476,086 , GRCh38.p12 chr3: 106,441,422-123,757,239	, ADPRH, 270 more genes
nsv4083806	copy number variation	1	nstd166	human		GRCh37.p13 chr3: 107,585,179-107,585,926 , GRCh38.p12 chr3: 107,866,332-107,867,079	LINC00635
nsv4077471	copy number variation	1	nstd166	human		GRCh37.p13 chr3: 107,569,381-107,569,443 , GRCh38.p12 chr3: 107,850,534-107,850,596	LINC00635
nsv3968046	copy number variation	1	nstd168	human		GRCh38 chr3: 107,827,281-107,857,594 , GRCh37.p13 chr3: 107,546,128-107,576,441	LINC00635
nsv3922717	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 95,002,154-146,895,858 , GRCh38 chr3: 93,800,620-145,695,381 , GRCh37 chr3: 93,519,464-145,413,168	OR7E53P, HSPA8P9, 794 more genes
nsv3921388	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 107,653,029-110,467,033 , GRCh38 chr3: 106,451,492-109,265,496 , GRCh37 chr3: 106,170,339-108,984,343	BBX, CCDC54-AS1, 43 more genes
nsv3918981	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446	LINC02614, LINC02054, 1469 more genes
nsv3918661	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 95,088,205-124,418,220 , GRCh37 chr3: 93,605,515-122,935,530 , GRCh38 chr3: 93,886,671-123,216,683	MTCO2P29, GAP43, 401 more genes
nsv3917160	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 95,021,157-118,088,593 , GRCh38 chr3: 93,819,623-116,887,056 , GRCh37 chr3: 93,538,467-116,605,903	ATP6V1A, RPS10P4, 297 more genes
nsv3913722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 103,411,064-109,324,749 , GRCh38 chr3: 103,692,220-109,605,902 , NCBI36 chr3: 104,893,754-110,807,439	MTND4P16, LOC105374029, 64 more genes
nsv3913319	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 105,822,754-117,295,421 , GRCh38 chr3: 104,621,220-116,093,884 , GRCh37 chr3: 104,340,064-115,812,731	TAGLN3, LINC00635, 151 more genes
nsv3911662	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 102,633,427-117,731,277 , GRCh37.p13 chr3: 101,150,737-116,248,587 , GRCh38.p12 chr3: 101,431,893-116,529,740	SIDT1, PPIAP15, 188 more genes

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Number of Variants: 20

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Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 152

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Number of Variants: 20

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