trps1[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
nsv3888667	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 116,426,231-116,635,884 , GRCh38.p12 chr8: 115,414,003-115,623,657	TRPS1
nsv3888932	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 115,414,022-115,587,000 , GRCh37.p13 chr8: 116,426,250-116,599,227	TRPS1
nsv6637405	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 116,454,726-116,614,300 , GRCh38.p12 chr8: 115,442,498-115,602,073	TRPS1
nsv3914187	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 116,482,735-116,583,432 , GRCh37 chr8: 116,413,559-116,514,256 , GRCh38 chr8: 115,401,331-115,502,029	TRPS1
nsv4455286	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 116,415,097-116,502,268 , GRCh38.p12 chr8: 115,402,869-115,490,041	TRPS1
nsv4682996	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 116,599,208-116,599,851 , GRCh38.p12 chr8: 115,586,981-115,587,624	TRPS1
nsv6312896	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 116,635,808-116,635,864 , GRCh38.p12 chr8: 115,623,581-115,623,637	TRPS1
nsv997137	copy number variation	1	nstd45	human	Pathogenic	GRCh38.p12 chr8: 115,408,496-115,669,028 , GRCh37 chr8: 116,420,724-116,681,255	TRPS1
nsv3877818	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr8: 116,469,546-116,616,099 , GRCh38 chr8: 115,418,453-115,603,872	TRPS1
nsv6312895	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr8: 116,599,208-116,635,864 , GRCh38.p12 chr8: 115,586,981-115,623,637	TRPS1
nsv3884528	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 116,616,080-116,635,884 , GRCh38 chr8: 115,603,853-115,623,657	TRPS1
nsv4685630	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr8: 116,613,171-116,616,277 , GRCh38 chr8: 115,600,944-115,604,050	TRPS1
nsv3903026	copy number variation	1	nstd102	human	Benign	GRCh37 chr8: 116,420,327-116,648,565 , GRCh38.p12 chr8: 115,408,099-115,636,338	TRPS1
nsv3921522	copy number variation	1	nstd102	human	Likely benign	GRCh38 chr8: 115,485,621-115,514,859 , GRCh37 chr8: 116,497,848-116,527,086 , NCBI36 chr8: 116,567,024-116,596,262	TRPS1
nsv4675254	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 116,515,769-116,541,758 , GRCh38.p12 chr8: 115,503,542-115,529,531	TRPS1
nsv3874880	copy number variation	1	nstd102	human	not provided	GRCh37 chr8: 116,426,250-116,430,557 , GRCh38 chr8: 115,414,022-115,418,329	TRPS1
nsv4729562	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 116,104,969-116,678,186 , GRCh38.p12 chr8: 115,092,740-115,665,959	TRPS1
nsv3896144	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 115,656,140-116,918,407 , GRCh38.p12 chr8: 114,643,911-115,906,182	TRPS1, CARS1P2, 3 more genes
nsv6637224	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 112,234,557-133,668,379 , GRCh38.p12 chr8: 111,222,328-132,656,133	TRPS1, RNU4-37P, 220 more genes
nsv3876297	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 114,508,086-129,040,004 , GRCh38.p12 chr8: 113,495,857-128,027,758	TRPS1, ZHX1-C8orf76, 172 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 70

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 70

Page of 4

Number of Variants: 20

Page of 4

Supplemental Content

Find related data

Search details

Recent activity