stambpl1[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
nsv3903394	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 90,680,186-90,774,157 , GRCh38.p12 chr10: 88,920,429-89,014,400	STAMBPL1, FAS-AS1, 3 more genes
nsv7137209	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639	STAMBPL1, RNU7-12P, 1876 more genes
nsv3920295	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 81,675,342-135,374,737 , GRCh37.p13 chr10: 81,685,362-135,524,747 , GRCh38.p12 chr10: 79,925,606-133,787,422	STAMBPL1, EIF2S2P3, 895 more genes
nsv6637542	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 82,595,472-93,542,416 , GRCh38.p12 chr10: 80,835,716-91,782,659	STAMBPL1, IFIT6P, 166 more genes
nsv3891568	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 83,379,241-93,219,169 , GRCh38.p12 chr10: 81,619,485-91,459,412	STAMBPL1, NAPGP1, 157 more genes
nsv6634458	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 83,533,660-91,913,077 , GRCh38.p12 chr10: 81,773,904-90,153,320	STAMBPL1, IFIT5, 140 more genes
nsv6637868	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 89,823,147-96,056,941 , GRCh38.p12 chr10: 88,063,390-94,297,184	STAMBPL1, RPS27P1, 118 more genes
nsv4729624	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 88,685,387-92,144,296 , GRCh38.p12 chr10: 86,925,630-90,384,539	STAMBPL1, LOC105378414, 84 more genes
nsv4681949	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 89,622,918-90,708,693 , GRCh38.p12 chr10: 87,863,161-88,948,936	STAMBPL1, LIPM, 22 more genes
nsv4682162	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 90,530,602-91,087,835 , GRCh38.p12 chr10: 88,770,845-89,328,078	STAMBPL1, MIR4679-2, 17 more genes
nsv3906389	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996	STAMBPL1, LOC100419870, 2105 more genes
nsv3891157	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 98,087-135,477,883 , GRCh38.p12 chr10: 52,147-133,740,558	STAMBPL1, AGAP14P, 2097 more genes
nsv3902271	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639	STAMBPL1, ANXA11, 2085 more genes
nsv3891958	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 93,297-135,378,918 , GRCh38.p12 chr10: 47,357-133,565,414	STAMBPL1, TUBB8, 2085 more genes
nsv7137211	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639	STAMBPL1, EXOC6, 1906 more genes
nsv3891070	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 69,040,366-93,194,993 , GRCh38.p12 chr10: 67,280,608-91,435,236	STAMBPL1, NRG3-AS1, 441 more genes
nsv3920479	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 84,434,981-89,150,802 , NCBI36 chr10: 86,184,717-90,900,539 , GRCh37 chr10: 86,194,737-90,910,559	STAMBPL1, LOC105378406, 86 more genes
nsv3907664	copy number variation	1	nstd102	human	drug response	GRCh37 chr10: 42,347,406-135,534,747 , GRCh38.p12 chr10: 42,101,241-133,787,422	STAMBPL1, SHOC2, 1487 more genes
nsv3894450	copy number variation	1	nstd102	human	drug response	GRCh37 chr10: 85,557,432-105,804,295 , GRCh38.p12 chr10: 83,797,676-104,044,537	STAMBPL1, HPS1, 422 more genes
nsv4455319	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 90,510,448-91,086,868 , GRCh38.p12 chr10: 88,750,691-89,327,111	STAMBPL1, PTCD2P2, 18 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 23

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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