wac[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
nsv4456506	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 28,862,876-28,916,803 , GRCh38.p12 chr10: 28,573,947-28,627,874	WAC
nsv5672681	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 28,904,915-28,906,395 , GRCh38 chr10: 28,615,986-28,617,466	WAC
nsv3318993	copy number variation	1	nstd45	human	Pathogenic	GRCh38.p12 chr10: 28,532,588-28,623,112 , GRCh37 chr10: 28,821,517-28,912,041	WAC, WAC-AS1
nsv6314302	complex chromosomal rearrangement	6	nstd102	human	Pathogenic	GRCh37 chr3: 149,332,307-149,332,307 , GRCh37 chr3: 154,453,976-154,453,976 , GRCh37 chr3: 149,332,307-149,332,307 , GRCh37 chr3: 154,453,975-154,453,975 , GRCh37 chr7: 12,374,295-12,374,295 , GRCh37 chr7: 12,374,296-12,374,296 , GRCh37 chr10: 28,823,742-28,823,742 , GRCh37 chr10: 11,940,759-11,940,759 , GRCh37 chr10: 102,794,873-102,794,873 , GRCh37 chr10: 102,794,873-102,794,873 , GRCh37 chr10: 11,940,757-11,940,757 , GRCh37 chr10: 28,823,741-28,823,741 , GRCh38.p12 chr10: 101,035,116-101,035,116 , GRCh38.p12 chr10: 28,534,812-28,534,812 , GRCh38.p12 chr10: 11,898,758-11,898,758 , GRCh38.p12 chr10: 101,035,116-101,035,116 , GRCh38.p12 chr10: 11,898,760-11,898,760 , GRCh38.p12 chr10: 28,534,813-28,534,813 , GRCh38.p12 chr3: 149,614,520-149,614,520 , GRCh38.p12 chr3: 149,614,520-149,614,520 , GRCh38.p12 chr3: 154,736,187-154,736,187 , GRCh38.p12 chr3: 154,736,186-154,736,186 , GRCh38.p12 chr7: 12,334,669-12,334,669 , GRCh38.p12 chr7: 12,334,670-12,334,670	WAC, SFXN3, 2 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	WAC, 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	WAC, 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	WAC, TRIAP1P1, 70 more genes
nsv6291211	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 27,204,530-29,105,882 , GRCh38.p12 chr10: 26,915,601-28,816,953	WAC, LINC02673, 44 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	WAC, 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	WAC, 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	WAC, 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	WAC, 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	WAC, 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	WAC, 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	WAC, 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	WAC, 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	WAC, 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	WAC, 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	WAC, LOC100420467, 709 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	WAC, C1QL3, 774 more genes

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Number of Variants: 20

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