dbVar for Gene (Select 131118) - 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
nsv5438448	copy number variation	1	nstd206	human		GRCh38 chr3: 180,981,724-180,981,812 , GRCh37.p13 chr3: 180,699,512-180,699,600	DNAJC19, FXR1
nsv4921067	copy number variation	1	nstd200	human		GRCh38 chr3: 180,985,054-180,985,276 , GRCh37.p13 chr3: 180,702,842-180,703,064	DNAJC19
nsv4798801	copy number variation	1	nstd200	human		GRCh37 chr3: 180,702,842-180,703,064 , GRCh38.p12 chr3: 180,985,054-180,985,276	DNAJC19
nsv4769329	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 180,102,701-181,991,155 , GRCh38.p12 chr3: 180,384,913-182,273,367	TTC14, RPL32P10, 24 more genes
nsv4728751	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 179,016,729-181,527,320 , GRCh38.p12 chr3: 179,298,941-181,809,532	PEX5L, NDUFB5, 33 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
nsv4674507	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 180,510,432-181,562,798 , GRCh38.p12 chr3: 180,792,644-181,845,010	DNAJC19, FXR1, 13 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
nsv4096678	copy number variation	1	nstd166	human		GRCh37.p13 chr3: 180,702,842-180,703,064 , GRCh38.p12 chr3: 180,985,054-180,985,276	DNAJC19
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
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
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
nsv3913254	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 175,313,014-183,652,825 , GRCh37.p13 chr3: 173,830,320-182,170,131 , GRCh38.p12 chr3: 174,112,530-182,452,343	RNU6-486P, TBL1XR1, 88 more genes

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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 86

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Number of Variants: 20

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