dbVar for Gene (Select 1427) - 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
nsv5453639	copy number variation	1	nstd206	human		GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871	, MIR922, 587 more genes
nsv4728604	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 182,877,291-186,830,759 , GRCh38.p12 chr3: 183,159,503-187,112,971	LOC105374253, GPS2P2, 111 more genes
nsv4728363	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 186,048,846-186,298,472 , GRCh38.p12 chr3: 186,331,057-186,580,683	LINC02051, CRYGS, 5 more genes
nsv4683580	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 186,256,465-187,009,440 , GRCh38.p12 chr3: 186,538,676-187,291,652	RPL39P19, FETUB, 32 more genes
nsv4674680	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 169,617,690-190,593,854 , GRCh38.p12 chr3: 169,899,902-190,876,065	RNU6-1120P, LOC105374262, 323 more genes
nsv4674249	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 185,879,162-187,446,035 , GRCh38.p12 chr3: 186,161,373-187,728,247	RTP1, RPL29P9, 43 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
nsv3922577	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 184,561,415-187,178,796 , GRCh38 chr3: 184,843,627-187,461,008 , NCBI36 chr3: 186,044,109-188,661,490	SNORA63, ADIPOQ-AS1, 59 more genes
nsv3922385	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 177,369,007-199,329,651 , GRCh37 chr3: 175,886,313-197,845,254 , GRCh38 chr3: 176,168,525-198,118,383	LINC02053, RTP4, 414 more genes
nsv3920662	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 178,729,187-199,321,446 , GRCh37.p13 chr3: 177,246,493-197,837,049 , GRCh38.p12 chr3: 177,528,705-198,110,178	RN7SKP265, RPL24P6, 401 more genes
nsv3920607	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 187,082,628-197,946,692 , GRCh37.p13 chr3: 185,599,934-196,462,295 , GRCh38.p12 chr3: 185,882,146-196,735,424	FGF12, RFC4, 212 more genes
nsv3918982	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 167,885,356-197,837,049 , NCBI36 chr3: 169,368,050-199,321,446 , GRCh38 chr3: 168,167,568-198,110,178	EIF4G1, LOC105374248, 515 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
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
nsv3916294	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr3: 187,209,491-187,755,373 , GRCh37 chr3: 185,726,797-186,272,679 , GRCh38 chr3: 186,009,008-186,554,890	DGKG, ETV5, 6 more genes
nsv3915488	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 185,203,637-197,837,049 , NCBI36 chr3: 186,686,331-199,321,446 , GRCh38 chr3: 185,485,849-198,110,178	SNAR-I, RPL23AP93, 260 more genes
nsv3914762	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr3: 168,918,444-189,565,754 , GRCh37 chr3: 167,435,750-188,083,060 , GRCh38 chr3: 167,717,962-188,365,272	ACTL6A, AHSG, 325 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

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Has Clinical Interpretation

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Items: 1 to 20 of 102

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Number of Variants: 20

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