usb1[All Fields] AND 1[has_clinical] - 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
nsv3906951	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 58,034,200-58,034,489 , GRCh38.p12 chr16: 58,000,296-58,000,585	USB1, ZNF319
nsv3891356	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr16: 58,050,710-58,079,499 , GRCh38.p12 chr16: 58,016,806-58,045,595	USB1, MMP15
nsv3906560	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 58,030,650-58,034,489 , GRCh38.p12 chr16: 57,996,746-58,000,585	USB1, ZNF319
nsv3891054	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 58,034,030-58,077,521 , GRCh38.p12 chr16: 58,000,126-58,043,617	USB1, MMP15, 1 more genes
nsv3916542	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 55,457,477-63,841,622 , NCBI36 chr16: 54,048,890-62,433,027 , GRCh37 chr16: 55,491,389-63,875,526	USB1, CES1, 139 more genes
nsv3908644	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 56,950,941-60,203,590 , GRCh38.p12 chr16: 56,917,029-60,169,686	USB1, ADGRG1, 75 more genes
nsv7095031	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr16: 56,226,148-58,768,132 , GRCh38.p12 chr16: 56,192,236-58,734,228	USB1, MT1B, 92 more genes
nsv7094589	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 57,016,057-58,768,132 , GRCh38.p12 chr16: 56,982,145-58,734,228	USB1, SLC38A7, 58 more genes
nsv3906108	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224	USB1, CKLF, 1882 more genes
nsv3904593	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973	USB1, LOC100128079, 1879 more genes
nsv3901410	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287	USB1, LINC02175, 1877 more genes
nsv3909417	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867	USB1, PRSS53, 1868 more genes
nsv3892266	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr16: 85,881-90,155,062 , GRCh38.p12 chr16: 35,881-90,088,654	USB1, FTLP14, 1868 more genes
nsv3921269	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 31,893,599-88,822,254 , GRCh37.p13 chr16: 31,986,098-90,294,753 , GRCh38.p12 chr16: 31,974,777-90,228,345	USB1, LOC105371237, 985 more genes
nsv6314755	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654	USB1, ATMIN, 826 more genes
nsv3915506	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 51,490,596-88,682,563 , GRCh38 chr16: 52,899,183-90,088,654 , GRCh37 chr16: 52,933,095-90,155,062	USB1, CFAP69P1, 716 more genes
nsv3891306	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 57,051,473-89,797,669 , GRCh38.p12 chr16: 57,017,561-89,731,261	USB1, LOC107984894, 613 more genes
nsv3895555	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 34,197,492-64,509,054 , GRCh38.p12 chr16: 34,963,121-64,475,151	USB1, RSPRY1, 362 more genes
nsv3918521	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 48,276,933-66,993,116 , GRCh37 chr16: 49,719,432-68,435,615 , GRCh38 chr16: 49,685,521-68,401,712	USB1, CYLD-AS2, 342 more genes
nsv3893486	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 54,416,050-72,453,266 , GRCh38.p12 chr16: 54,382,138-72,419,367	USB1, ZNF19, 375 more genes

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 41

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Number of Variants: 20

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