abi1[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 19

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Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6308907	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 26,986,641-27,035,402 , GRCh38.p12 chr10: 26,697,712-26,746,473	ABI1, PDSS1, 1 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	ABI1, RNU7-12P, 1876 more genes
nsv3911283	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 27,111,945-30,537,855 , NCBI36 chr10: 27,151,951-30,577,861 , GRCh38 chr10: 26,823,016-30,248,926	ABI1, YME1L1, 72 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	ABI1, 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	ABI1, 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	ABI1, 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	ABI1, 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	ABI1, 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	ABI1, 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	ABI1, 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	ABI1, RPL36AP55, 418 more genes
nsv3910289	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 25,484,473-26,963,308 , NCBI36 chr10: 25,813,408-27,292,243 , GRCh37 chr10: 25,773,402-27,252,237	ABI1, RNU6-946P, 22 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	ABI1, 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	ABI1, LOC100420467, 709 more genes
nsv3891361	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr10: 26,318,337-27,889,818 , GRCh38.p12 chr10: 26,029,408-27,600,889	ABI1, PTCHD3, 31 more genes
nsv3898766	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr10: 26,344,939-27,889,818 , GRCh38.p12 chr10: 26,056,010-27,600,889	ABI1, RNU6-490P, 31 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	ABI1, C1QL3, 774 more genes
nsv7093630	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 26,993,586-28,391,597 , GRCh38.p12 chr10: 26,704,657-28,102,668	ABI1, PDSS1, 30 more genes
nsv6637568	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 27,065,576-27,549,923 , GRCh38.p12 chr10: 26,776,647-27,260,994	ABI1, RNU7-12P, 10 more genes

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abi1[All Fields] AND 1[has_clinical] (20)
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