plpp1[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
nsv3883312	copy number variation	1	nstd102	human	Benign	GRCh37 chr5: 54,824,594-54,826,054 , GRCh38.p12 chr5: 55,528,766-55,530,226	PLPP1, RNF138P1
nsv3888754	copy number variation	1	nstd102	human	Benign	GRCh37 chr5: 54,824,876-54,826,054 , GRCh38.p12 chr5: 55,529,048-55,530,226	PLPP1, RNF138P1
nsv3871458	copy number variation	1	nstd102	human	Benign	GRCh37 chr5: 54,824,594-54,825,744 , GRCh38.p12 chr5: 55,528,766-55,529,916	PLPP1, RNF138P1
nsv3875866	copy number variation	1	nstd102	human	Benign	GRCh37 chr5: 54,740,571-55,010,963 , GRCh38.p12 chr5: 55,444,743-55,715,135	PLPP1, RNF138P1, 3 more genes
nsv4457202	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 54,623,265-54,815,203 , GRCh38.p12 chr5: 55,327,437-55,519,375	PLPP1, LOC100419851, 3 more genes
nsv3889848	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719	PLPP1, MEGF10, 2080 more genes
nsv3923429	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 49,584,189-62,445,597 , NCBI36 chr5: 49,619,946-62,481,353 , GRCh38 chr5: 50,288,355-63,149,770	PLPP1, ISCA1P1, 163 more genes
nsv3922909	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 50,462,100-55,862,985 , GRCh37 chr5: 49,757,934-55,158,813 , NCBI36 chr5: 49,793,691-55,194,570	PLPP1, HMGB1P47, 72 more genes
nsv7097148	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 52,285,299-56,189,507 , GRCh38.p12 chr5: 52,989,469-56,893,680	PLPP1, RPL37P25, 69 more genes
nsv3886374	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028	PLPP1, LOC105374618, 2499 more genes
nsv3871533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343	PLPP1, PCDHGC5, 2492 more genes
nsv3875235	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788	PLPP1, SPEF2, 2490 more genes
nsv3911585	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 75,149-73,744,306 , GRCh38 chr5: 22,149-74,412,725 , GRCh37 chr5: 22,149-73,708,550	PLPP1, LINC02241, 878 more genes
nsv3920391	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 35,201,559-61,903,141 , GRCh37 chr5: 35,201,661-61,198,968 , NCBI36 chr5: 35,237,418-61,234,725	PLPP1, KRT18P56, 290 more genes
nsv3878755	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr5: 53,784,524-54,985,838 , GRCh38.p12 chr5: 54,488,694-55,690,010	PLPP1, MIR449C, 26 more genes
nsv3889039	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr5: 54,635,880-55,019,572 , GRCh38.p12 chr5: 55,340,052-55,723,744	PLPP1, MTREX, 6 more genes
nsv4436202	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379	PLPP1, RNU1-150P, 1757 more genes
nsv3912593	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr5: 332,389-180,837,866 , GRCh37.p13 chr5: 279,389-180,905,260 , GRCh38.p12 chr5: 279,274-181,478,259	PLPP1, LOC105378993, 2492 more genes
nsv3913817	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 45,566,963-55,802,320 , GRCh38 chr5: 45,566,861-56,506,493 , NCBI36 chr5: 45,602,720-55,838,077	PLPP1, LINC02118, 90 more genes
nsv3917640	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr5: 54,359,842-55,271,282 , GRCh38 chr5: 55,028,257-55,939,697 , GRCh37 chr5: 54,324,085-55,235,525	PLPP1, MIR449C, 24 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 21

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Number of Variants: 20

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Supplemental Content

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Search details

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