taf3[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
nsv3900913	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 7,981,522-7,996,740 , GRCh38.p12 chr10: 7,939,559-7,954,777	TAF3
nsv6314205	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 7,943,586-8,120,292 , GRCh38.p12 chr10: 7,901,623-8,078,329	TAF3, GATA3, 2 more genes
nsv3898054	copy number variation	1	nstd102	human	Likely pathogenic	GRCh38.p12 chr10: 8,014,326-8,076,702 , GRCh37 chr10: 8,056,289-8,118,665	TAF3, GATA3, 2 more genes
nsv3900212	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 7,846,569-7,989,049 , GRCh38.p12 chr10: 7,804,606-7,947,086	TAF3, ATP5F1C, 1 more genes
nsv3908158	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 7,837,730-7,904,170 , GRCh38.p12 chr10: 7,795,767-7,862,207	TAF3, ATP5F1C, 1 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	TAF3, 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	TAF3, 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	TAF3, 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	TAF3, 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	TAF3, 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	TAF3, 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	TAF3, TRV-TAC3-1, 163 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	TAF3, AKR1C6P, 121 more genes
nsv4455884	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 8,011,156-9,996,086 , GRCh38.p12 chr10: 7,969,193-9,954,123	TAF3, LOC105376396, 22 more genes
nsv6314032	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 8,046,788-9,979,612 , GRCh38.p12 chr10: 8,004,825-9,937,649	TAF3, LOC105376398, 22 more genes
nsv3904739	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 7,377,293-9,129,131 , GRCh38.p12 chr10: 7,335,331-9,087,168	TAF3, ITIH2, 27 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	TAF3, 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	TAF3, 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	TAF3, 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	TAF3, TUBB8, 2085 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 39

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Number of Variants: 20

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Supplemental Content

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