gtf2f2[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
nsv3910270	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 18,445,862-114,327,173 , NCBI36 chr13: 10,098,739-114,110,750 , GRCh37 chr13: 19,020,001-115,085,141	GTF2F2, RNU6-71P, 1332 more genes
nsv3924528	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 41,516,434-115,085,141 , GRCh38 chr13: 40,942,298-114,340,331 , NCBI36 chr13: 40,414,434-114,123,908	GTF2F2, LOC105370271, 925 more genes
nsv3898603	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 42,457,841-91,796,698 , GRCh38.p12 chr13: 41,883,705-91,144,444	GTF2F2, RNY4P30, 575 more genes
nsv3918812	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 44,967,523-92,738,168 , NCBI36 chr13: 44,439,658-92,188,422 , GRCh37 chr13: 45,541,658-93,390,421	GTF2F2, SRSF1P1, 541 more genes
nsv6314117	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 36,376,204-80,681,753 , GRCh38.p12 chr13: 35,802,067-80,107,618	GTF2F2, RBM26, 591 more genes
nsv3913649	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 41,143,820-85,137,552 , GRCh37 chr13: 41,717,956-85,711,687 , NCBI36 chr13: 40,615,956-84,609,688	GTF2F2, RPL21P108, 539 more genes
nsv3915679	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 31,271,865-70,046,105 , GRCh38 chr13: 30,697,728-69,471,973 , NCBI36 chr13: 30,169,865-68,944,106	GTF2F2, CCDC70, 524 more genes
nsv3923911	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 38,438,363-68,537,920 , GRCh38 chr13: 37,864,226-67,963,788 , NCBI36 chr13: 37,336,363-67,435,921	GTF2F2, MLNR, 422 more genes
nsv3907596	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,946,120-62,698,217 , GRCh38.p12 chr13: 32,371,983-62,124,084	GTF2F2, TPT1, 434 more genes
nsv3915542	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 37,351,455-63,530,009 , NCBI36 chr13: 36,249,455-62,428,010 , GRCh38 chr13: 36,777,318-62,955,876	GTF2F2, LINC02338, 393 more genes
nsv6290319	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 45,819,046-63,910,212 , GRCh38.p12 chr13: 45,244,911-63,336,079	GTF2F2, CNMD, 241 more genes
nsv3921404	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 31,592,297-49,065,340 , GRCh38 chr13: 31,018,160-48,491,204 , NCBI36 chr13: 30,490,297-47,963,341	GTF2F2, MIR8079, 280 more genes
nsv3923636	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr13: 37,986,314-50,897,351 , GRCh37 chr13: 39,088,314-51,999,350 , GRCh38 chr13: 38,514,177-51,425,214	GTF2F2, TUSC8, 251 more genes
nsv6314198	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 44,573,371-53,324,137 , GRCh38.p12 chr13: 43,999,235-52,750,002	GTF2F2, PCNPP5, 189 more genes
nsv3924173	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 43,505,396-49,983,668 , NCBI36 chr13: 42,977,532-49,455,805 , GRCh37 chr13: 44,079,532-50,557,804	GTF2F2, PCNPP5, 131 more genes
nsv6315495	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403	GTF2F2, RNU6-80P, 1334 more genes
nsv6289999	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403	GTF2F2, LINC00363, 1334 more genes
nsv3897246	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 19,031,237-115,107,157 , GRCh38.p12 chr13: 18,457,097-114,341,682	GTF2F2, NT5CP3, 1334 more genes
nsv3924676	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 18,456,040-114,340,285 , GRCh37 chr13: 19,030,180-115,105,760 , NCBI36 chr13: 17,928,180-114,123,862	GTF2F2, GRTP1, 1334 more genes
nsv5564510	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053	GTF2F2, RN7SL272P, 1333 more genes

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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 50

Page of 3

Number of Variants: 20

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Supplemental Content

Find related data

Search details

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