bud13[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 17

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Number of Variants: 17

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv5380796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397	BUD13, FAUP4, 2031 more genes
nsv4455554	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 104,101,411-116,680,918 , GRCh38.p12 chr11: 104,230,683-116,810,202	BUD13, LINC02732, 198 more genes
nsv3893233	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576	BUD13, LOC105376598, 2842 more genes
nsv3900144	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169	BUD13, RTN3, 2833 more genes
nsv3908873	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576	BUD13, IGHMBP2, 2829 more genes
nsv6315537	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576	BUD13, PYGM, 2125 more genes
nsv3898361	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 71,588,805-116,680,918 , GRCh38.p12 chr11: 71,877,759-116,810,202	BUD13, SESN3, 694 more genes
nsv3922253	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 100,219,331-134,910,140 , NCBI36 chr11: 99,724,541-134,415,350 , GRCh38 chr11: 100,348,599-135,040,246	BUD13, RPS27P19, 655 more genes
nsv6289927	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 104,288,964-134,937,416 , GRCh38.p12 chr11: 104,418,236-135,067,522	BUD13, IGSF9B, 592 more genes
nsv3912905	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 112,864,326-131,189,315 , GRCh37 chr11: 112,832,130-131,059,210 , NCBI36 chr11: 112,240,259-130,564,420	BUD13, SLC37A2, 416 more genes
nsv6291074	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 112,375,478-128,785,742 , GRCh38.p12 chr11: 112,504,755-128,915,847	BUD13, ZW10, 378 more genes
nsv3913230	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 113,444,446-120,648,921 , NCBI36 chr11: 112,820,378-120,024,840 , GRCh37 chr11: 113,315,168-120,519,630	BUD13, ARHGEF12, 169 more genes
nsv3909122	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 115,215,434-120,559,928 , GRCh38.p12 chr11: 115,344,715-120,689,219	BUD13, LOC107984393, 136 more genes
nsv3914316	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 115,812,352-117,422,156 , GRCh38 chr11: 116,436,425-118,046,231 , GRCh37 chr11: 116,307,142-117,916,946	BUD13, LOC653303, 31 more genes
nsv4674572	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr11: 114,433,313-131,230,466 , GRCh38.p12 chr11: 114,562,591-131,360,571	BUD13, ACRV1, 382 more genes
nsv6290834	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 85,422,071-118,022,671 , GRCh38.p12 chr11: 85,711,028-118,151,956	BUD13, CARD17P, 480 more genes
nsv3911601	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr11: 115,023,598-116,957,808 , GRCh37 chr11: 115,518,388-117,452,598 , GRCh38 chr11: 115,647,670-117,581,883	BUD13, ZPR1, 32 more genes

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