cstf2t[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
nsv6314082	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 53,134,455-53,811,118 , GRCh38.p12 chr10: 51,374,695-52,051,358	CSTF2T, PRKG1
nsv4675742	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 53,144,955-53,811,118 , GRCh38.p12 chr10: 51,385,195-52,051,358	CSTF2T, PRKG1
nsv7093877	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 53,227,463-53,769,653 , GRCh38.p12 chr10: 51,467,703-52,009,893	CSTF2T, PRKG1
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	CSTF2T, RNU7-12P, 1876 more genes
nsv4675455	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 50,250,603-69,256,083 , GRCh38.p12 chr10: 45,931,517-67,496,325	CSTF2T, MRLN, 242 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	CSTF2T, 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	CSTF2T, 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	CSTF2T, 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	CSTF2T, 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	CSTF2T, 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	CSTF2T, 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	CSTF2T, SLC9A3P3, 476 more genes
nsv3921181	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 41,927,641-68,830,439 , GRCh38 chr10: 42,112,187-67,400,675 , GRCh37 chr10: 42,607,635-69,160,433	CSTF2T, AGAP6, 338 more genes
nsv3916253	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 42,884,294-52,265,317 , NCBI36 chr10: 42,699,748-53,695,083 , GRCh37 chr10: 43,379,742-54,025,077	CSTF2T, PTPN20CP, 198 more genes
nsv3972371	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr10: 49,390,457-60,061,643 , GRCh38.p12 chr10: 45,931,517-58,301,883	CSTF2T, CHAT, 156 more genes
nsv3923539	inversion	1	nstd102	human	Likely pathogenic	GRCh38.p12 chr10: 43,115,743-59,903,521 , GRCh37 chr10: 43,611,191-61,663,279	CSTF2T, ALOX5, 248 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	CSTF2T, SHOC2, 1487 more genes
nsv3917648	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 52,727,283-55,468,943 , GRCh38 chr10: 50,967,523-53,709,183 , NCBI36 chr10: 52,397,289-55,138,949	CSTF2T, LOC105378310, 17 more genes
nsv3901291	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 52,752,503-57,406,199 , GRCh38.p12 chr10: 50,992,743-55,646,439	CSTF2T, LOC105378308, 23 more genes

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