dbVar for Gene (Select 106478996) - 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
nsv6112714	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 127,927,712-136,889,323 , GRCh38.p12 chr3: 128,208,869-137,170,481	RNU6-789P, FAM86HP, 169 more genes
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
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
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
nsv3921297	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 133,918,512-145,986,275 , GRCh38 chr3: 132,716,978-144,784,743 , GRCh37 chr3: 132,435,822-144,503,585	BFSP2, YWHAQP6, 169 more genes
nsv3920834	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr3: 127,308,312-142,119,621 , GRCh38 chr3: 126,106,779-140,918,089 , GRCh37 chr3: 125,825,622-140,636,931	NCK1-DT, LOC107986126, 271 more genes
nsv3920279	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 129,817,243-143,381,624 , GRCh37 chr3: 129,536,086-143,100,466 , NCBI36 chr3: 131,018,776-144,583,156	NPHP3-AS1, RNA5SP142, 218 more genes
nsv3920044	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 132,972,567-136,894,498 , GRCh37 chr3: 132,691,411-136,613,340 , NCBI36 chr3: 134,174,101-138,096,030	TOPBP1, LOC105374123, 56 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
nsv3918871	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 130,401,265-139,005,019 , NCBI36 chr3: 131,602,799-140,206,551 , GRCh37 chr3: 130,120,109-138,723,861	FOXL2, NPHP3, 132 more genes
nsv3914757	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 131,018,776-142,626,687 , GRCh38 chr3: 129,817,243-141,425,155 , GRCh37 chr3: 129,536,086-141,143,997	CLSTN2-AS1, COPB2, 177 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
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
nsv3872147	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr3: 132,642,704-136,360,844 , GRCh38.p12 chr3: 132,923,860-136,642,002	EPHB1, PCCB, 51 more genes
esv4011097	complex chromosomal rearrangement	6	estd236	human		GRCh37 chr3: 125,695,543-174,724,062 , GRCh38.p12 chr3: 125,976,700-175,006,272	, AADAC, 733 more genes
nsv3168810	inversion	1	nstd158	human		GRCh37 chr3: 115,360,357-196,043,925 , GRCh38.p12 chr3: 115,641,510-196,317,054	, AADAC, 1298 more genes
nsv2737271	copy number variation	1	nstd130	human		NCBI36 chr3: 125,676,839-199,298,372 , GRCh37.p13 chr3: 124,194,149-197,813,975 , GRCh38.p12 chr3: 124,475,302-198,087,104	, LOC105374108, 1221 more genes
nsv2206684	short tandem repeat	4	nstd128	human		GRCh37 chr3: 133,427,615-133,427,627 , GRCh38.p12 chr3: 133,708,771-133,708,783	INHCAP, TF, 1 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

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 81

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Number of Variants: 20

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