hras[All Fields] AND 1[has_clinical] - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7137059	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr11: 530,419-530,474 , GRCh38 chr11: 530,419-530,474	HRAS, LRRC56
nsv6137846	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 528,484-534,377 , GRCh38.p12 chr11: 528,484-534,377 , GRCh38.p12 chr11\|NT_187586.1: 58,125-64,018	HRAS, LRRC56
nsv4682767	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 532,636-534,322 , GRCh38.p12 chr11: 532,636-534,322 , GRCh38.p12 chr11\|NT_187586.1: 62,277-63,963	HRAS, LRRC56
nsv4685920	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 532,573-534,003 , GRCh38 chr11: 532,573-534,003	HRAS, LRRC56
nsv6309368	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 532,636-533,328 , GRCh38.p12 chr11: 532,636-533,328 , GRCh38.p12 chr11\|NT_187586.1: 62,277-62,969	HRAS, LRRC56
nsv4769296	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 532,631-534,375 , GRCh38.p12 chr11: 532,631-534,375 , GRCh38.p12 chr11\|NT_187586.1: 62,272-64,016	HRAS, LRRC56
nsv1398187	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr11: 532,631-534,375 , GRCh37 chr11: 532,631-534,375	HRAS, LRRC56
nsv4683704	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 532,616-534,342 , GRCh38.p12 chr11\|NT_187586.1: 62,257-63,983 , GRCh38.p12 chr11: 532,616-534,342	HRAS, LRRC56
nsv4454318	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 532,626-534,332 , GRCh38 chr11: 532,626-534,332	HRAS, LRRC56
nsv5564369	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 532,636-533,622 , GRCh38.p12 chr11: 532,636-533,622 , GRCh38.p12 chr11\|NT_187586.1: 62,277-63,263	HRAS, LRRC56
nsv6309369	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 533,443-534,322 , GRCh38.p12 chr11\|NT_187586.1: 63,084-63,963 , GRCh38.p12 chr11: 533,443-534,322	HRAS, LRRC56
nsv5380886	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 532,630-532,761 , GRCh38.p12 chr11: 532,630-532,761 , GRCh38.p12 chr11\|NT_187586.1: 62,271-62,402	HRAS, LRRC56
nsv3874766	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr11: 532,631-532,755 , GRCh37 chr11: 532,631-532,755	HRAS, LRRC56
nsv4681966	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 534,206-534,328 , GRCh38.p12 chr11: 534,206-534,328 , GRCh38.p12 chr11\|NT_187586.1: 63,847-63,969	HRAS, LRRC56
nsv7093222	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr11: 533,463-533,464 , GRCh37 chr11: 533,463-533,464	HRAS, LRRC56
nsv7094089	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr11: 532,636-554,276 , GRCh38.p12 chr11: 532,636-554,276 , GRCh38.p12 chr11\|NT_187586.1: 62,277-83,916	HRAS, LRRC56, 1 more genes
nsv6634327	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 499,700-5,279,697 , GRCh37.p13 chr11: 499,700-5,300,927	HRAS, SNORA54, 219 more genes
nsv7137204	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 268,586-748,873 , GRCh38.p12 chr11: 268,586-748,873	HRAS, PKP3, 32 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	HRAS, LOC105376598, 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	HRAS, RTN3, 2833 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:

Search results

Items: 1 to 20 of 57

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Search details

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

Search results

Items: 1 to 20 of 57

Page of 3

Number of Variants: 20

Page of 3

Supplemental Content

Find related data

Search details

Recent activity