adk[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
nsv3918868	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr10: 74,195,087-74,468,002 , NCBI36 chr10: 75,624,851-75,897,766 , GRCh37 chr10: 75,954,845-76,227,760	ADK, TIMM9P1, 2 more genes
nsv7093803	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 75,936,631-76,468,203 , GRCh38.p12 chr10: 74,176,873-74,708,445	ADK, MRPL35P3, 6 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	ADK, 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	ADK, 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	ADK, 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	ADK, SLC25A16, 204 more genes
nsv3905190	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 75,542,067-79,428,995 , GRCh38.p12 chr10: 73,782,309-77,669,237	ADK, TIMM9P1, 47 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	ADK, CAMK2G, 73 more genes
nsv7093731	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 76,349,020-78,317,046 , GRCh38.p12 chr10: 74,589,262-76,557,288	ADK, SAMD8, 25 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	ADK, 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	ADK, 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	ADK, 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	ADK, 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	ADK, 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	ADK, BMS1P4-AGAP5, 471 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	ADK, 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	ADK, LINC02640, 231 more genes
nsv3904905	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 75,922,676-76,611,753 , GRCh38.p12 chr10: 74,162,918-74,851,995	ADK, KAT6B, 8 more genes
nsv3897169	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 75,890,021-76,356,834 , GRCh38.p12 chr10: 74,130,263-74,597,076	ADK, AP3M1, 5 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	ADK, SHOC2, 1487 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 23

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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