dcaf13[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
nsv3922470	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 102,183,491-110,139,893 , GRCh38 chr8: 101,171,263-109,127,664 , NCBI36 chr8: 102,252,667-110,209,069	DCAF13, HMGB1P46, 109 more genes
nsv3913241	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 101,260,812-107,606,071 , GRCh38 chr8: 100,179,408-106,524,667 , GRCh37 chr8: 101,191,636-107,536,895	DCAF13, LRP12, 113 more genes
nsv3919996	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 102,897,047-108,368,371 , GRCh38 chr8: 101,884,819-107,356,143 , NCBI36 chr8: 102,966,223-108,437,547	DCAF13, BAALC-AS1, 79 more genes
nsv3910618	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 102,281,230-106,883,502 , GRCh38 chr8: 101,199,826-105,802,098 , GRCh37 chr8: 102,212,054-106,814,326	DCAF13, LINC03047, 84 more genes
nsv3915173	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 3,938-146,274,826 , GRCh37.p13 chr8: 13,938-146,304,022 , GRCh38.p12 chr8: 63,938-145,078,636	DCAF13, RN7SL474P, 2109 more genes
nsv3901821	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 10,213-146,293,414 , GRCh38.p12 chr8: 60,213-145,068,028	DCAF13, TBC1D31, 2109 more genes
nsv4349554	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385	DCAF13, LOC101929488, 2105 more genes
nsv3916777	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-146,295,771 , GRCh38 chr8: 208,048-145,070,385 , NCBI36 chr8: 148,048-146,266,575	DCAF13, RPL5P22, 2105 more genes
nsv3898123	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr8: 158,049-146,295,771 , GRCh38.p12 chr8: 208,049-145,070,385	DCAF13, SPAG1, 2105 more genes
nsv3908608	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 164,984-146,293,414 , GRCh38.p12 chr8: 214,984-145,068,028	DCAF13, LINC01617, 2105 more genes
nsv3893757	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,991-146,280,828 , GRCh38.p12 chr8: 208,991-145,055,442	DCAF13, LOC105375890, 2105 more genes
nsv3923310	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098	DCAF13, LOC112268023, 2105 more genes
nsv3914307	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 191,605-146,280,167 , GRCh38 chr8: 241,605-145,054,781 , NCBI36 chr8: 181,605-146,250,971	DCAF13, LOC107986897, 2104 more genes
nsv3919282	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 191,530-146,280,020 , GRCh38 chr8: 241,530-145,054,634 , NCBI36 chr8: 181,530-146,250,824	DCAF13, MIR4662B, 2104 more genes
nsv3919200	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 241,530-145,049,449 , GRCh37 chr8: 191,530-146,274,835 , NCBI36 chr8: 181,530-146,245,639	DCAF13, LOC112268023, 2103 more genes
nsv3906425	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 12,490,999-146,295,771 , GRCh38.p12 chr8: 12,633,490-145,070,385	DCAF13, LOC112268016, 1819 more genes
nsv3915762	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 21,193,313-146,266,575 , GRCh38 chr8: 21,291,522-145,070,385 , GRCh37 chr8: 21,149,033-146,295,771	DCAF13, LOC105375693, 1718 more genes
nsv4456811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385	DCAF13, TERF1, 1511 more genes
nsv3916438	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 46,942,962-140,297,737 , NCBI36 chr8: 47,062,127-140,366,919 , GRCh38 chr8: 46,031,340-139,285,494	DCAF13, NDUFS5P6, 1152 more genes
nsv6634360	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385	DCAF13, WASHC5, 1028 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 48

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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