arhgap21[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 16

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Number of Variants: 16

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3897951	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 24,847,361-24,870,596 , GRCh38.p12 chr10: 24,558,432-24,581,667	ARHGAP21
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	ARHGAP21, RNU7-12P, 1876 more genes
nsv3910612	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 24,400,270-25,639,569 , GRCh38 chr10: 24,111,341-25,350,640 , NCBI36 chr10: 24,440,276-25,679,575	ARHGAP21, KIAA1217, 13 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	ARHGAP21, 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	ARHGAP21, 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	ARHGAP21, 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	ARHGAP21, 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	ARHGAP21, EXOC6, 1906 more genes
nsv3904390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 100,026-50,961,640 , GRCh38.p12 chr10: 54,086-49,753,594	ARHGAP21, LINC00700, 806 more genes
nsv3920796	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 62,842-35,729,127 , GRCh37.p13 chr10: 72,842-35,689,121 , GRCh38.p12 chr10: 26,906-35,400,193	ARHGAP21, EPC1-AS1, 559 more genes
nsv6313952	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 6,273,934-34,732,521 , GRCh38.p12 chr10: 6,231,971-34,443,593	ARHGAP21, RPL36AP55, 418 more genes
nsv3917667	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 224,406-26,628,907 , GRCh38 chr10: 90,205-26,339,978 , NCBI36 chr10: 126,145-26,668,913	ARHGAP21, RN7SKP241, 389 more genes
nsv3911634	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr10: 19,417,096-33,061,227 , GRCh37 chr10: 19,377,090-33,021,221 , GRCh38 chr10: 19,088,161-32,732,293	ARHGAP21, BMI1, 221 more genes
nsv3920598	copy number variation	1	nstd102	human	Benign	NCBI36 chr10: 4,636,926-47,125,152 , GRCh38 chr10: 4,604,734-48,074,662 , GRCh37 chr10: 4,646,926-47,531,169	ARHGAP21, LOC100420467, 709 more genes
nsv3899385	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 24,628,319-26,747,630 , GRCh38.p12 chr10: 24,339,390-26,458,701	ARHGAP21, GPR158-AS1, 22 more genes
nsv6290893	copy number variation	1	nstd102	human	not provided	GRCh37 chr10: 135,655-47,688,677 , GRCh38.p12 chr10: 89,715-47,923,579	ARHGAP21, C1QL3, 774 more genes

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arhgap21[All Fields] AND 1[has_clinical] (17)
dbVar
S.albus mitochondrial 12S rRNA gene (partial)
S.albus mitochondrial 12S rRNA gene (partial)
gi|1160260|emb|X95028.1|

Nucleotide

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