mss51[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 17

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	MSS51, RNU7-12P, 1876 more genes
nsv3922335	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 60,196,226-76,174,974 , GRCh38 chr10: 58,436,466-74,415,216 , NCBI36 chr10: 59,866,232-75,844,980	MSS51, UNC5B-AS1, 250 more genes
nsv3917822	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 63,402,579-75,296,099 , GRCh37 chr10: 65,162,339-77,055,857 , NCBI36 chr10: 64,832,345-76,725,863	MSS51, MYL6P3, 220 more genes
nsv6314185	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 68,735,254-78,885,714 , GRCh38.p12 chr10: 66,975,496-77,125,956	MSS51, SLC25A16, 204 more genes
nsv3910545	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 74,150,392-77,042,138 , GRCh38 chr10: 72,720,628-75,612,374 , GRCh37 chr10: 74,480,386-77,372,132	MSS51, CAMK2G, 73 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	MSS51, 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	MSS51, 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	MSS51, 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	MSS51, 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	MSS51, EXOC6, 1906 more genes
nsv3924859	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 52,159,133-88,896,941 , GRCh38 chr10: 50,729,367-87,147,204 , GRCh37 chr10: 52,489,127-88,906,961	MSS51, BMS1P4-AGAP5, 471 more genes
nsv3917047	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 42,500,760-75,145,672 , GRCh37 chr10: 43,180,754-75,475,666 , GRCh38 chr10: 42,685,306-73,715,908	MSS51, SLC9A3P3, 476 more genes
nsv3891070	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 69,040,366-93,194,993 , GRCh38.p12 chr10: 67,280,608-91,435,236	MSS51, NRG3-AS1, 441 more genes
nsv3917966	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 68,626,331-80,851,819 , GRCh37 chr10: 68,956,325-81,181,813 , GRCh38 chr10: 67,196,567-79,422,057	MSS51, LINC02640, 231 more genes
nsv3891946	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 75,089,777-75,359,997 , GRCh38.p12 chr10: 73,330,019-73,600,239	MSS51, PPP3CB-AS1, 7 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	MSS51, SHOC2, 1487 more genes
nsv3894848	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 75,179,409-76,009,153 , GRCh38.p12 chr10: 73,419,651-74,249,395	MSS51, AGAP5, 27 more genes

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