fra10ac1[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
nsv6634488	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 95,459,755-95,462,674 , GRCh38 chr10: 93,699,998-93,702,917	FRA10AC1
nsv6634697	delins	1	nstd102	human	Pathogenic	GRCh38 chr10: 93,695,674-93,708,392 , GRCh37.p13 chr10: 95,455,431-95,468,149	FRA10AC1
nsv4682142	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr10: 95,415,517-95,459,863 , GRCh38.p12 chr10: 93,655,760-93,700,106	FRA10AC1, PDE6C
nsv4455513	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 95,421,794-95,473,856 , GRCh38.p12 chr10: 93,662,037-93,714,099	FRA10AC1, PDE6C
nsv3894051	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 95,301,338-95,475,336 , GRCh38.p12 chr10: 93,541,581-93,715,579	FRA10AC1, RBP4, 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	FRA10AC1, 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	FRA10AC1, EIF2S2P3, 895 more genes
nsv3911437	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 93,181,201-101,356,779 , NCBI36 chr10: 94,930,948-103,106,526 , GRCh37 chr10: 94,940,958-103,116,536	FRA10AC1, SLF2, 171 more genes
nsv3894877	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 93,908,171-101,809,723 , GRCh38.p12 chr10: 92,148,414-100,049,966	FRA10AC1, RNY3P12, 146 more genes
nsv3908115	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 92,667,881-98,970,384 , GRCh38.p12 chr10: 90,908,124-97,210,627	FRA10AC1, EXOC6, 118 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	FRA10AC1, RPS27P1, 118 more genes
nsv3912487	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 94,386,437-99,514,859 , GRCh38 chr10: 92,626,680-97,755,102 , NCBI36 chr10: 94,376,417-99,504,849	FRA10AC1, ENTPD1-AS1, 105 more genes
nsv7098887	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 93,249,133-97,616,970 , GRCh38.p12 chr10: 91,489,376-95,857,213	FRA10AC1, LGI1, 79 more genes
nsv3914138	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 94,403,676-97,230,894 , GRCh38 chr10: 92,643,919-95,471,137 , NCBI36 chr10: 94,393,656-97,220,884	FRA10AC1, RPL7AP52, 51 more genes
nsv3901659	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 93,186,527-95,820,286 , GRCh38.p12 chr10: 91,426,770-94,060,529	FRA10AC1, NHP2P1, 48 more genes
nsv4682030	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr10: 94,921,066-95,557,580 , GRCh38.p12 chr10: 93,161,309-93,797,823	FRA10AC1, LGI1, 11 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	FRA10AC1, 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	FRA10AC1, 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	FRA10AC1, 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	FRA10AC1, TUBB8, 2085 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 27

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 27

Page of 2

Number of Variants: 20

Page of 2

Supplemental Content

Find related data

Search details

Recent activity