pyroxd2[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
nsv4456005	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 100,067,156-100,257,755 , GRCh38.p12 chr10: 98,307,399-98,497,998	PYROXD2, HPS1, 5 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	PYROXD2, 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	PYROXD2, EIF2S2P3, 895 more genes
nsv3911437	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 93,181,201-101,356,779 , NCBI36 chr10: 94,930,948-103,106,526 , GRCh37 chr10: 94,940,958-103,116,536	PYROXD2, SLF2, 171 more genes
nsv3894877	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 93,908,171-101,809,723 , GRCh38.p12 chr10: 92,148,414-100,049,966	PYROXD2, RNY3P12, 146 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	PYROXD2, 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	PYROXD2, 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	PYROXD2, 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	PYROXD2, 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	PYROXD2, 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	PYROXD2, 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	PYROXD2, UROS, 667 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	PYROXD2, LOC102723665, 360 more genes
nsv3908203	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 99,923,079-100,191,207 , GRCh38.p12 chr10: 98,163,322-98,431,450	PYROXD2, HPS1, 5 more genes
nsv4729159	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 100,015,920-100,234,444 , GRCh38.p12 chr10: 98,256,163-98,474,687	PYROXD2, LOXL4, 6 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	PYROXD2, 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	PYROXD2, HPS1, 422 more genes
nsv4674930	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 100,138,329-100,488,874 , GRCh38.p12 chr10: 98,378,572-98,729,117	PYROXD2, HPS1-AS1, 4 more genes
nsv3920535	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr10: 100,063,955-100,305,454 , GRCh37.p13 chr10: 100,073,965-100,315,464 , GRCh38.p12 chr10: 98,314,208-98,555,707	PYROXD2, HPS1-AS1, 5 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	PYROXD2, ABCC2, 160 more genes

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Has Clinical Interpretation

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Items: 20

Number of Variants: 20

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