dbVar for Gene (Select 10218) - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7099176	copy number variation	1	nstd231	human		GRCh38.p12 chr1: 10,224,807-12,488,948 , GRCh37 chr1: 10,284,865-12,549,002	TNFRSF8, CLCN6, 64 more genes
nsv7098827	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 4,481,271-20,530,242 , GRCh38.p12 chr1: 4,421,211-20,203,749	LOC107985467, LINC01777, 386 more genes
nsv7096008	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 9,304,994-12,569,078 , GRCh38.p12 chr1: 9,244,935-12,509,024	NMNAT1, DISP3, 91 more genes
nsv7095738	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 10,753,911-11,854,615 , GRCh38.p12 chr1: 10,693,854-11,794,558	MAD2L2, HSPE1P24, 33 more genes
nsv7095692	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 10,698,999-11,907,741 , GRCh38.p12 chr1: 10,638,942-11,847,684	MTHFR, UBIAD1, 36 more genes
nsv7095543	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 9,770,514-11,264,780 , GRCh38.p12 chr1: 9,710,456-11,204,723	DFFA, ANGPTL7, 38 more genes
nsv7057525	inversion	1	nstd229	human		GRCh38 chr1: 7,829,944-15,116,659 , GRCh37.p13 chr1: 7,890,004-15,443,155	PEX14, RNU6-304P, 187 more genes
nsv7052549	inversion	1	nstd229	human		GRCh38 chr1: 8,322,830-13,737,741 , GRCh37.p13 chr1: 8,382,890-14,064,236	MIR4632, PLOD1, 166 more genes
nsv7048193	inversion	1	nstd229	human		GRCh38 chr1: 9,469,567-16,279,388 , GRCh37.p13 chr1: 9,529,626-16,605,883	PRAMEF36P, HNRNPCL3, 193 more genes
nsv7047983	inversion	1	nstd229	human		GRCh38 chr1: 5,346,988-12,521,611 , GRCh37.p13 chr1: 5,407,048-12,581,655	THAP3, UBIAD1, 165 more genes
nsv7046461	inversion	1	nstd229	human		GRCh38 chr1: 5,352,168-12,521,473 , GRCh37.p13 chr1: 5,412,228-12,581,517	LINC02606, C1orf127, 165 more genes
nsv6657761	copy number variation	1	nstd229	human		GRCh38 chr1: 9,535,063-15,753,073 , GRCh37.p13 chr1: 9,595,122-16,079,568	SLC25A34-AS1, TMEM274P, 173 more genes
nsv6639839	copy number variation	1	nstd229	human		GRCh38 chr1: 11,088,601-11,213,200 , GRCh37.p13 chr1: 11,148,658-11,273,257	MTOR-AS1, EXOSC10-AS1, 4 more genes
nsv6638770	copy number variation	1	nstd229	human		GRCh38 chr1: 10,461,501-12,236,800 , GRCh37.p13 chr1: 10,521,558-12,296,857	RN7SL614P, CFL1P6, 57 more genes
nsv6637093	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 849,467-12,448,956 , GRCh38.p12 chr1: 914,087-12,388,897	VWA1, CEP104, 311 more genes
nsv6636785	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 6,758,933-19,287,770 , GRCh38.p12 chr1: 6,698,873-18,961,276	GPR157, MST1L, 313 more genes
nsv6315241	copy number variation	1	nstd102	human	Likely pathogenic	GRCh38 chr1: 10,115,497-16,283,149 , GRCh37.p13 chr1: 10,175,555-16,609,644	CASP9, CD24P1, 173 more genes
nsv6290672	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 849,466-17,525,065 , GRCh38.p12 chr1: 914,086-17,198,570	RPL9P11, FAM131C2P, 466 more genes
nsv6133884	copy number variation	1	nstd213	human		GRCh37 chr1: 8,430,000-11,640,001 , GRCh38.p12 chr1: 8,369,940-11,579,944	RERE, CA6, 79 more genes
nsv5557473	sequence alteration	1	nstd206	human		GRCh38 chr1: 10,919,048-11,710,696 , GRCh37.p13 chr1: 10,979,105-11,770,753	, ANGPTL7, 26 more genes

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

Send to:

Links from Gene

Items: 1 to 20 of 128

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Recent activity

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

Links from Gene

Items: 1 to 20 of 128

Page of 7

Number of Variants: 20

Page of 7

Supplemental Content

Find related data

Recent activity