jcad[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
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	JCAD, 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	JCAD, YME1L1, 72 more genes
nsv3915584	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 27,046,685-30,228,891 , GRCh37 chr10: 27,335,614-30,517,820 , NCBI36 chr10: 27,375,620-30,557,826	JCAD, TRIAP1P1, 70 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	JCAD, 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	JCAD, 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	JCAD, 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	JCAD, 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	JCAD, 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	JCAD, 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	JCAD, 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	JCAD, RPL36AP55, 418 more genes
nsv3921533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 28,056,899-30,335,014 , NCBI36 chr10: 28,096,905-30,375,020 , GRCh38 chr10: 27,767,970-30,046,085	JCAD, ODAD2, 48 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	JCAD, 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	JCAD, LOC100420467, 709 more genes
nsv3905007	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr10: 29,849,273-30,352,152 , GRCh38.p12 chr10: 29,560,344-30,063,223	JCAD, LOC107984218, 10 more genes
nsv3900511	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 30,346,833-30,678,471 , GRCh38.p12 chr10: 30,057,904-30,389,542	JCAD, EEF1A1P39, 10 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	JCAD, C1QL3, 774 more genes
nsv4674851	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 29,204,926-30,604,037 , GRCh38.p12 chr10: 28,915,997-30,315,108	JCAD, EEF1A1P39, 25 more genes
nsv4674836	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 30,138,613-31,334,200 , GRCh38.p12 chr10: 29,849,684-31,045,271	JCAD, MTPAP, 24 more genes

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