pkia[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
nsv4456100	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 79,485,514-79,512,626 , GRCh38.p12 chr8: 78,573,279-78,600,391	PKIA, LOC105375911
nsv3918712	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr8: 78,888,738-79,708,815 , GRCh37.p13 chr8: 78,726,183-79,546,260 , GRCh38.p12 chr8: 77,813,948-78,634,025	PKIA, PKIA-AS1, 2 more genes
nsv3914059	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 78,677,666-92,851,513 , GRCh38 chr8: 77,765,431-91,839,285 , NCBI36 chr8: 78,840,221-92,920,689	PKIA, RN7SL107P, 176 more genes
nsv3922848	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 74,954,174-86,710,947 , GRCh37 chr8: 74,791,620-86,523,695 , GRCh38 chr8: 73,879,385-85,611,466	PKIA, MITA1, 139 more genes
nsv6315163	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 75,904,944-87,097,083 , GRCh38.p12 chr8: 74,992,709-86,084,854	PKIA, ZNF704, 137 more genes
nsv6313579	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 77,906,471-88,917,707 , GRCh38.p12 chr8: 76,994,235-87,905,479	PKIA, LOC105375915, 143 more genes
nsv3915614	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 74,431,535-83,567,817 , NCBI36 chr8: 74,594,089-83,730,372 , GRCh38 chr8: 73,519,300-82,655,582	PKIA, DSTNP3, 116 more genes
nsv3895973	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 75,197,438-81,685,526 , GRCh38.p12 chr8: 74,285,203-80,773,291	PKIA, MIR2052, 72 more genes
nsv3918656	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 75,817,543-82,252,186 , NCBI36 chr8: 75,980,098-82,414,741 , GRCh38 chr8: 74,905,308-81,339,951	PKIA, ZFHX4, 71 more genes
nsv3903585	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 77,751,515-83,516,216 , GRCh38.p12 chr8: 76,839,279-82,603,981	PKIA, LOC105375926, 79 more genes
nsv3890890	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 74,942,333-80,413,867 , GRCh38.p12 chr8: 74,030,098-79,501,632	PKIA, ZC2HC1A, 46 more genes
nsv3923698	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 79,617,219-84,706,949 , GRCh37.p13 chr8: 79,454,664-84,544,394 , GRCh38.p12 chr8: 78,542,429-83,632,159	PKIA, RPS26P34, 77 more genes
nsv3907856	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 77,345,003-79,544,235 , GRCh38.p12 chr8: 76,432,768-78,632,000	PKIA, HIGD1AP18, 12 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	PKIA, 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	PKIA, 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	PKIA, 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	PKIA, 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	PKIA, 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	PKIA, 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	PKIA, LOC105375890, 2105 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 43

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Number of Variants: 20

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