U2[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
nsv4456660	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 15,745,414-15,961,746 , GRCh38.p12 chr12: 15,592,480-15,808,812	EPS8, PTPRO, 2 more genes
nsv5380796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397	FAUP4, MMP7, 2031 more genes
nsv3916249	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189	H3P40, EEF1B2P1, 1616 more genes
nsv3919468	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189	RNU6-18P, GOLGA8K, 1442 more genes
nsv3911811	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577	PRPSAP1, CACNG1, 1350 more genes
nsv4729092	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 86,962,053-102,531,392 , GRCh38.p12 chr15: 86,418,822-101,981,189	CHD2, MIR11181, 272 more genes
nsv4675149	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 87,189,245-102,429,112 , GRCh38.p12 chr15: 86,646,014-101,888,909	TTLL13, LINC00052, 264 more genes
nsv6634456	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 10,853,887-24,103,810 , GRCh38.p12 chr12: 10,701,288-23,950,876	TAS2R15P, LOC105369673, 209 more genes
nsv3908429	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 90,346,994-102,354,798 , GRCh38.p12 chr15: 89,803,763-101,814,595	RPL31P55, LOC100421368, 201 more genes
nsv3899918	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 92,197,136-102,354,857 , GRCh38.p12 chr15: 91,653,906-101,814,654	SNRPCP18, SPATA41, 148 more genes
nsv6112780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 92,335,751-102,399,741 , GRCh38.p12 chr15: 91,792,521-101,859,538	LOC105371009, ST8SIA2, 149 more genes
nsv3919064	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 91,542,950-100,200,996 , GRCh38 chr15: 93,198,717-101,843,270 , GRCh37 chr15: 93,741,946-102,383,473	LOC105371032, SPATA8-AS1, 126 more genes
nsv3918825	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 94,348,261-101,867,081 , GRCh38 chr15: 93,805,032-101,326,876 , NCBI36 chr15: 92,149,265-99,684,604	LOC440311, LOC100507472, 107 more genes
nsv3922914	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 92,814,458-100,338,915 , GRCh37.p13 chr15: 95,013,454-102,521,392 , GRCh38.p12 chr15: 94,470,225-101,981,189	OR4F14P, RNA5SP401, 124 more genes
nsv3897684	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 95,136,822-102,045,577 , GRCh38.p12 chr15: 94,593,593-101,505,374	ARRDC4, LOC105371001, 98 more genes
nsv6313944	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 94,836,128-101,302,111 , GRCh38.p12 chr15: 94,292,899-100,761,906	LINC01582, LRRC28, 85 more genes
nsv4675174	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 11,737,824-16,780,886 , GRCh38.p12 chr12: 11,584,890-16,627,952	LOC107001063, RN7SKP162, 89 more genes
nsv3915189	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr12: 12,388,842-15,540,422 , GRCh37 chr12: 12,541,776-15,693,356 , NCBI36 chr12: 12,433,043-15,584,623	GUCY2C, GSG1, 63 more genes
nsv3893233	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576	LOC105376598, OSBPL9P2, 2842 more genes
nsv3900144	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169	RTN3, KRTAP5-13P, 2833 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 136

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Number of Variants: 20

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