armh3[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
nsv3897808	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 103,816,369-103,828,060 , GRCh38.p12 chr10: 102,056,612-102,068,303	ARMH3, HPS6
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	ARMH3, 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	ARMH3, EIF2S2P3, 895 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	ARMH3, 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	ARMH3, 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	ARMH3, 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	ARMH3, 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	ARMH3, EXOC6, 1906 more genes
nsv3905489	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 93,283,493-135,427,143 , GRCh38.p12 chr10: 91,523,736-133,613,639	ARMH3, LOC105378476, 688 more genes
nsv3890046	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 94,346,520-135,427,143 , GRCh38.p12 chr10: 92,586,763-133,613,639	ARMH3, UROS, 667 more genes
nsv3921919	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 100,600,492-133,622,588 , GRCh37 chr10: 102,360,249-135,436,092 , NCBI36 chr10: 102,350,239-135,286,082	ARMH3, MIR4295, 508 more genes
nsv3898332	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 103,288,313-135,512,075 , GRCh38.p12 chr10: 101,528,556-133,774,750	ARMH3, NPS, 503 more genes
nsv3923769	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 100,194,215-132,432,797 , GRCh37 chr10: 101,953,972-134,246,301 , NCBI36 chr10: 101,943,962-134,096,291	ARMH3, LOC105378493, 477 more genes
nsv3909942	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 96,872,364-118,383,651 , GRCh38 chr10: 95,112,607-116,776,637 , NCBI36 chr10: 96,862,354-118,526,138	ARMH3, LOC102723665, 360 more genes
nsv6314273	complex chromosomal rearrangement	9	nstd102	human	Pathogenic	GRCh37 chr10: 43,970,076-43,970,076 , GRCh37 chr10: 74,987,633-74,987,633 , GRCh37 chr10: 103,789,246-103,789,246 , GRCh37 chr10: 103,989,173-103,989,173 , GRCh37 chr10: 43,970,076-43,970,076 , GRCh37 chr10: 70,451,274-70,451,274 , GRCh37 chr10: 98,467,287-98,467,287 , GRCh37 chr10: 103,789,246-103,789,246 , GRCh37 chr10: 43,841,488-43,841,488 , GRCh37 chr10: 46,951,966-46,951,966 , GRCh37 chr10: 70,451,274-70,451,274 , GRCh37 chr10: 98,467,287-98,467,287 , GRCh37 chr10: 98,644,903-98,644,903 , GRCh37 chr10: 98,644,903-98,644,903 , GRCh37 chr10: 43,841,488-43,841,488 , GRCh37 chr10: 46,950,701-46,950,701 , GRCh37 chr10: 74,987,633-74,987,633 , GRCh37 chr10: 103,989,173-103,989,173 , GRCh38.p12 chr10: 43,474,628-43,474,628 , GRCh38.p12 chr10: 46,597,651-46,597,651 , GRCh38.p12 chr10: 68,691,517-68,691,517 , GRCh38.p12 chr10: 96,707,530-96,707,530 , GRCh38.p12 chr10: 96,885,146-96,885,146 , GRCh38.p12 chr10: 102,029,489-102,029,489 , GRCh38.p12 chr10: 43,346,040-43,346,040 , GRCh38.p12 chr10: 46,598,916-46,598,916 , GRCh38.p12 chr10: 96,707,530-96,707,530 , GRCh38.p12 chr10: 96,885,146-96,885,146 , GRCh38.p12 chr10: 102,229,416-102,229,416 , GRCh38.p12 chr10: 43,346,040-43,346,040 , GRCh38.p12 chr10: 68,691,517-68,691,517 , GRCh38.p12 chr10: 73,227,875-73,227,875 , GRCh38.p12 chr10: 102,229,416-102,229,416 , GRCh38.p12 chr10: 43,474,628-43,474,628 , GRCh38.p12 chr10: 73,227,875-73,227,875 , GRCh38.p12 chr10: 102,029,489-102,029,489	ARMH3, LOC105378289, 10 more genes
nsv3907664	copy number variation	1	nstd102	human	drug response	GRCh37 chr10: 42,347,406-135,534,747 , GRCh38.p12 chr10: 42,101,241-133,787,422	ARMH3, SHOC2, 1487 more genes
nsv3894450	copy number variation	1	nstd102	human	drug response	GRCh37 chr10: 85,557,432-105,804,295 , GRCh38.p12 chr10: 83,797,676-104,044,537	ARMH3, HPS1, 422 more genes
nsv4728795	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 103,582,453-103,931,269 , GRCh38.p12 chr10: 101,822,696-102,171,512	ARMH3, HPS6, 6 more genes
nsv3922274	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr10: 103,274,160-135,374,737 , GRCh37.p13 chr10: 103,284,170-135,524,747 , GRCh38.p12 chr10: 101,524,413-133,787,422	ARMH3, DPCD, 504 more genes
nsv7093904	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 99,344,461-105,992,004 , GRCh38.p12 chr10: 97,584,704-104,232,246	ARMH3, ABCC2, 160 more genes

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Items: 20

Number of Variants: 20

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