asb13[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
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	ASB13, 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	ASB13, HSPA14, 228 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	ASB13, IL9RP2, 232 more genes
nsv3890577	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 100,026-12,842,179 , GRCh38.p12 chr10: 54,086-12,800,180	ASB13, LOC105376364, 208 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	ASB13, LINC02656, 200 more genes
nsv3893746	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 136,361-8,850,609 , GRCh38.p12 chr10: 90,421-8,808,646	ASB13, TRV-TAC3-1, 163 more genes
nsv5672604	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 120,001-6,920,000 , GRCh38.p12 chr10: 74,061-6,878,038	ASB13, PITRM1-AS1, 133 more genes
nsv3924022	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 105,200-6,291,337 , GRCh38 chr10: 69,260-6,209,368 , GRCh37 chr10: 224,406-6,251,331	ASB13, LINC02561, 120 more genes
nsv3907813	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 2,593,113-8,484,746 , GRCh38.p12 chr10: 2,550,921-8,442,783	ASB13, AKR1C6P, 121 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	ASB13, 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	ASB13, 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	ASB13, 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	ASB13, TUBB8, 2085 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	ASB13, 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	ASB13, EPC1-AS1, 559 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	ASB13, 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	ASB13, 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	ASB13, 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	ASB13, LOC105376357, 264 more genes
nsv3915964	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 90,026-13,287,922 , GRCh38 chr10: 54,086-13,205,916 , GRCh37 chr10: 100,026-13,247,916	ASB13, LOC105376409, 217 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 37

Page of 2

Number of Variants: 20

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Supplemental Content

Find related data

Search details

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