usp13[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
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	USP13, RNU6-486P, 88 more genes
nsv6634512	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 179,547,548-182,152,788 , GRCh37.p13 chr3: 179,265,336-181,870,576	USP13, LOC105374243, 34 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	USP13, PEX5L, 33 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	USP13, RNU4-62P, 2880 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	USP13, NDUFB4, 2876 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	USP13, RPL23AP49, 2875 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	USP13, LINC02614, 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	USP13, LOC105374179, 785 more genes
nsv3874894	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 142,995,020-192,997,215 , GRCh38.p12 chr3: 143,276,178-193,279,426	USP13, RNU6-901P, 673 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	USP13, LOC105374260, 696 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	USP13, LINC02031, 647 more genes
nsv3913128	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 156,321,878-198,113,452 , NCBI36 chr3: 157,522,361-199,324,720 , GRCh37 chr3: 156,039,667-197,840,323	USP13, SNORA4, 644 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	USP13, RPL34P10, 625 more genes
nsv3871065	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 158,980,631-197,766,890 , GRCh38.p12 chr3: 159,262,842-198,040,019	USP13, LINC02048, 599 more genes
nsv3912173	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 167,337,691-199,336,383 , GRCh37 chr3: 165,854,997-197,851,986 , GRCh38 chr3: 166,137,209-198,125,115	USP13, LOC105374277, 540 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	USP13, EIF4G1, 515 more genes
nsv3871599	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 173,281,266-197,838,262 , GRCh38.p12 chr3: 173,563,476-198,111,391	USP13, LOC105374263, 436 more genes
nsv3889215	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 157,128,738-181,637,333 , GRCh38.p12 chr3: 157,410,949-181,919,545	USP13, NAALADL2, 274 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	USP13, LINC02053, 414 more genes
nsv3911190	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 176,157,699-197,845,254 , GRCh38 chr3: 176,439,911-198,118,383 , NCBI36 chr3: 177,640,393-199,329,651	USP13, RN7SL738P, 414 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

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 32

Page of 2

Number of Variants: 20

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Supplemental Content

Find related data

Search details

Recent activity