src[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
nsv3921364	copy number variation	1	nstd102	human	Likely benign	GRCh38 chr20: 47,390,946-47,514,274 , NCBI36 chr20: 45,453,097-45,576,425 , GRCh37 chr20: 46,019,690-46,143,018	NCOA3, RNU6-563P, 3 more genes
nsv6291731	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 46,147,529-46,438,075 , GRCh38.p12 chr20: 47,518,785-47,809,331	SULF2, NCOA3, 2 more genes
nsv6634330	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419	CYP1B1-AS1, LOC107985771, 1649 more genes
nsv3912723	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 30,288,202-45,731,170 , GRCh37.p13 chr20: 30,824,541-46,297,763 , GRCh38.p12 chr20: 32,236,738-47,669,019	SRC, LOC107985448, 370 more genes
nsv3910049	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 33,289,165-45,693,969 , GRCh37 chr20: 33,825,749-46,260,562 , GRCh38 chr20: 35,237,946-47,631,818	SRC, NDUFB4P10, 291 more genes
nsv3890734	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 22,656,029-28,601,557 , GRCh37 chr2: 22,802,524-28,748,053 , GRCh38 chr2: 22,579,652-28,525,186	MAPRE3-AS1, PPIL1P1, 142 more genes
nsv6290315	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 42,985,044-48,599,046 , GRCh38.p12 chr20: 44,356,404-49,982,509	PABPC1L, LOC107985401, 170 more genes
nsv3873411	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 19,905,995-24,762,790 , GRCh38.p12 chr2: 19,706,234-24,539,921	LOC100130841, PGAM1P6, 77 more genes
nsv6314937	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 22,439,520-25,608,211 , GRCh38.p12 chr2: 22,216,648-25,385,342	ITSN2, POMC, 50 more genes
nsv7096411	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 24,443,763-26,029,226 , GRCh38.p12 chr2: 24,220,894-25,806,357	LOC105369164, DTNB-AS1, 24 more genes
nsv6315390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305	LOC112268439, RNA5SP116, 3737 more genes
nsv3874648	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305	IGKV2OR2-10, LOC105374848, 3737 more genes
nsv3885544	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609	RNU6-674P, KANSL3, 3735 more genes
nsv3882615	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232	MTND2P22, LOC112268410, 3724 more genes
nsv3892750	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,961,294 , GRCh38.p12 chr20: 82,603-64,329,941	SRC, TGIF2-RAB5IF, 1314 more genes
nsv3905072	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,948,788 , GRCh38.p12 chr20: 82,603-64,317,435	SRC, LRRN4, 1313 more genes
nsv3895314	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr20: 61,569-62,915,555 , GRCh38.p12 chr20: 80,928-64,284,202	SRC, PKIG, 1311 more genes
nsv3896520	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,912,463 , GRCh38.p12 chr20: 82,603-64,281,110	SRC, COMMD7, 1311 more genes
nsv3920218	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118	SRC, MIR3646, 1310 more genes
nsv3908605	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 66,097-55,797,773 , GRCh38 chr2: 66,097-55,570,637 , NCBI36 chr2: 56,097-55,651,277	SLC35F6, LOC105374458, 801 more genes

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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 49

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Number of Variants: 20

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