dbVar for Gene (Select 402146) - 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
nsv5381765	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 138,173,683-162,494,699 , GRCh38.p12 chr3: 138,454,841-162,776,911	MBNL1-AS1, LOC107986138, 339 more genes
nsv5033132	inversion	1	nstd200	human		GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130	, LOC105374154, 433 more genes
nsv4912674	copy number variation	1	nstd200	human		GRCh38 chr3: 160,454,145-160,466,983 , GRCh37.p13 chr3: 160,171,933-160,184,771	B3GAT3P1, TRIM59-IFT80
nsv4684209	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 138,145,289-162,275,610 , GRCh38.p12 chr3: 138,426,447-162,557,822	MTAPP1, PLS1, 339 more genes
nsv4436220	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 158,567,751-160,802,139 , GRCh38.p12 chr3: 158,849,962-161,084,351	SCHIP1, KRT8P12, 29 more genes
nsv4380779	copy number variation	1	nstd173	human		GRCh37 chr3: 160,145,311-160,197,932 , GRCh38.p12 chr3: 160,427,523-160,480,144	SMC4, TRIM59-IFT80, 3 more genes
nsv4327395	inversion	1	nstd166	human		GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842	, ACTG1P1, 1039 more genes
nsv4327115	inversion	1	nstd166	human		GRCh37.p13 chr3: 131,882,701-162,233,318 , GRCh38.p12 chr3: 132,163,857-162,515,530	, ATP1B3, 446 more genes
nsv3919833	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 158,141,556-172,788,324 , NCBI36 chr3: 159,342,039-173,988,808 , GRCh37 chr3: 157,859,345-172,506,114	NMD3, TRV-AAC1-1, 173 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
nsv3918784	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 147,160,353-178,240,319 , GRCh38 chr3: 147,442,566-178,522,531 , NCBI36 chr3: 148,643,043-179,723,013	LOC105374167, LOC105374187, 394 more genes
nsv3918692	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 147,521,892-198,096,565 , GRCh37 chr3: 147,239,679-197,823,436 , NCBI36 chr3: 148,722,369-199,307,833	LOC105374179, LINC02038, 785 more genes
nsv3918149	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 155,836,230-197,851,986 , GRCh38 chr3: 156,118,441-198,125,115 , NCBI36 chr3: 157,318,924-199,336,383	LINC02031, PCBP2P4, 647 more genes
nsv3918066	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 152,100,512-198,118,383 , NCBI36 chr3: 153,300,991-199,329,651 , GRCh37 chr3: 151,818,301-197,845,254	LOC105374260, LOC105374174, 696 more genes
nsv3914686	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 158,493,861-199,345,995 , GRCh37 chr3: 157,011,167-197,861,598 , GRCh38 chr3: 157,293,378-198,134,727	RPL34P10, LOC105374264, 625 more genes
nsv3913128	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 156,321,878-198,113,452 , NCBI36 chr3: 157,522,361-199,324,720 , GRCh37 chr3: 156,039,667-197,840,323	SNORA4, MTCO3P38, 644 more genes
nsv3889228	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115	NDUFB4, LOC105374108, 2876 more genes
nsv3889215	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 157,128,738-181,637,333 , GRCh38.p12 chr3: 157,410,949-181,919,545	NAALADL2, LRRC31, 274 more genes
nsv3885606	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156	RNU4-62P, SEMA3B-AS1, 2880 more genes
nsv3880617	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391	RPL23AP49, DLEC1, 2875 more genes

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Has Clinical Interpretation

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Items: 1 to 20 of 107

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Number of Variants: 20

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