taf4[All Fields] AND 1[has_clinical] - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3903194	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 60,516,264-60,589,996 , GRCh38.p12 chr20\|NT_187623.1: 54,860-118,774 , GRCh38.p12 chr20: 61,941,208-62,014,940	TAF4, MIR1257, 1 more genes
nsv4457590	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 60,058,100-60,564,395 , GRCh38.p12 chr20: 61,483,044-61,989,339	TAF4, MIR1257, 2 more genes
nsv3892750	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,961,294 , GRCh38.p12 chr20: 82,603-64,329,941	TAF4, TGIF2-RAB5IF, 1314 more genes
nsv3905072	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,948,788 , GRCh38.p12 chr20: 82,603-64,317,435	TAF4, LRRN4, 1313 more genes
nsv3895314	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr20: 61,569-62,915,555 , GRCh38.p12 chr20: 80,928-64,284,202	TAF4, PKIG, 1311 more genes
nsv3896520	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,912,463 , GRCh38.p12 chr20: 82,603-64,281,110	TAF4, COMMD7, 1311 more genes
nsv3920218	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118	TAF4, MIR3646, 1310 more genes
nsv3915005	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 42,849,759-62,379,118 , GRCh37 chr20: 43,416,345-62,908,674 , GRCh38 chr20: 44,787,704-64,277,321	TAF4, FTLP1, 472 more genes
nsv6112778	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273	TAF4, LINC01742, 253 more genes
nsv3911673	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 54,773,088-62,908,674 , NCBI36 chr20: 54,206,495-62,379,118 , GRCh38 chr20: 56,198,032-64,277,321	TAF4, LOC105372709, 226 more genes
nsv4357849	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 54,143,747-62,194,881 , GRCh38.p12 chr20: 55,568,689-63,563,528	TAF4, RBM38, 192 more genes
nsv3910216	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 55,804,471-62,904,442 , NCBI36 chr20: 55,237,878-62,374,886 , GRCh38 chr20: 57,229,415-64,273,089	TAF4, GID8, 204 more genes
nsv4676332	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 55,743,522-62,032,989 , GRCh38.p12 chr20: 57,168,466-63,401,636	TAF4, BMP7, 153 more genes
nsv6314208	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 56,835,739-62,915,555 , GRCh38.p12 chr20: 58,260,683-64,284,202	TAF4, LOC105372698, 176 more genes
nsv4676181	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 56,788,101-62,762,405 , GRCh38.p12 chr20: 58,213,045-64,131,052	TAF4, LOC105372697, 174 more genes
nsv3916789	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 57,617,021-62,908,674 , GRCh38 chr20: 59,041,966-64,277,321 , NCBI36 chr20: 57,050,416-62,379,118	TAF4, RNU7-141P, 153 more genes
nsv3924353	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 59,335,000-62,379,123 , GRCh38 chr20: 61,326,549-64,277,326 , GRCh37 chr20: 59,901,605-62,908,679	TAF4, PPDPF, 126 more genes
nsv3896614	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 60,053,234-62,961,294 , GRCh38.p12 chr20: 61,478,178-64,329,941	TAF4, TNFRSF6B, 128 more genes
nsv3895755	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 60,063,645-62,961,294 , GRCh38.p12 chr20: 61,488,589-64,329,941	TAF4, LOC105372717, 128 more genes
nsv3894116	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr20: 51,542,616-62,915,555 , GRCh38.p12 chr20: 52,926,077-64,284,202	TAF4, ATP5F1E, 254 more genes

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

Send to:

Search results

Items: 1 to 20 of 27

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Search details

Recent activity

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

Page of 2

Number of Variants: 20

Page of 2

Supplemental Content

Find related data

Search details

Recent activity