ucma[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
nsv6314829	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr10: 13,233,315-13,234,242 , GRCh37 chr10: 13,275,315-13,276,242	UCMA
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	UCMA, RNU7-12P, 1876 more genes
nsv3914771	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 54,086-19,336,980 , NCBI36 chr10: 90,026-19,665,915 , GRCh37 chr10: 100,026-19,625,909	UCMA, COX6CP17, 302 more genes
nsv3884983	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 4,689,760-19,120,882 , GRCh38.p12 chr10: 4,647,568-18,831,953	UCMA, HSPA14, 228 more genes
nsv3911783	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 7,510,738-21,916,687 , GRCh37 chr10: 7,470,732-21,876,681 , GRCh38 chr10: 7,428,770-21,587,752	UCMA, LOC101928834, 192 more genes
nsv3918372	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 70,478-13,736,564 , GRCh37 chr10: 224,406-13,778,564 , NCBI36 chr10: 106,418-13,818,570	UCMA, IL9RP2, 232 more genes
nsv3911206	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 4,844,945-16,865,490 , NCBI36 chr10: 4,834,945-16,905,496 , GRCh38 chr10: 4,802,753-16,823,491	UCMA, LINC02656, 200 more genes
nsv5381768	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 9,137,489-17,227,168 , GRCh38.p12 chr10: 9,095,526-17,185,169	UCMA, PROSER2, 110 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	UCMA, 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	UCMA, 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	UCMA, 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	UCMA, 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	UCMA, 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	UCMA, 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	UCMA, 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	UCMA, RPL36AP55, 418 more genes
nsv3917667	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 224,406-26,628,907 , GRCh38 chr10: 90,205-26,339,978 , NCBI36 chr10: 126,145-26,668,913	UCMA, RN7SKP241, 389 more genes
nsv3924406	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 69,261-19,184,047 , GRCh37 chr10: 224,406-19,472,976 , NCBI36 chr10: 105,201-19,512,982	UCMA, WDR37, 302 more genes
nsv3920285	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 106,418-15,455,341 , GRCh37.p13 chr10: 116,418-15,415,335 , GRCh38.p12 chr10: 70,478-15,373,336	UCMA, NRBF2P5, 265 more genes
nsv4455607	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr10: 100,026-15,273,144 , GRCh38.p12 chr10: 54,086-15,231,145	UCMA, LOC105376357, 264 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 27

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Number of Variants: 20

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Supplemental Content

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