ftmt[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
nsv3877709	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr5: 121,187,653-121,188,438 , GRCh38.p12 chr5: 121,851,958-121,852,743	FTMT, LOC105379149
nsv3888288	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 121,095,875-121,247,735 , GRCh38.p12 chr5: 121,760,180-121,912,040	FTMT, LOC105379150, 2 more genes
nsv3889848	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719	FTMT, MEGF10, 2080 more genes
nsv3884357	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr5: 86,400,000-154,000,000 , GRCh38.p12 chr5: 87,104,183-154,620,440	FTMT, TXNDC15, 962 more genes
nsv3912937	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 105,955,289-155,551,397 , NCBI36 chr5: 105,983,188-155,483,975 , GRCh38 chr5: 106,619,588-156,124,387	FTMT, LINC01023, 783 more genes
nsv3915450	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 90,707,525-130,655,256 , NCBI36 chr5: 90,743,281-130,683,155 , GRCh38 chr5: 91,411,708-131,319,563	FTMT, MCTP1, 422 more genes
nsv3916468	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 89,670,423-127,412,115 , GRCh38 chr5: 90,374,606-128,076,423 , NCBI36 chr5: 89,706,179-127,440,014	FTMT, LOC105379149, 406 more genes
nsv3872414	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 100,607,918-125,900,735 , GRCh38.p12 chr5: 101,272,214-126,565,043	FTMT, ZRSR2P1, 248 more genes
nsv3924205	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 110,023,143-129,439,531 , GRCh38 chr5: 110,687,442-130,103,838 , NCBI36 chr5: 110,051,042-129,467,430	FTMT, CSNK1G3, 231 more genes
nsv3923804	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 107,644,164-125,113,490 , NCBI36 chr5: 107,672,063-125,141,389 , GRCh38 chr5: 108,308,463-125,777,797	FTMT, FABP5P6, 202 more genes
nsv3912712	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 116,677,122-132,686,163 , NCBI36 chr5: 116,040,717-132,049,754 , GRCh37 chr5: 116,012,818-132,021,855	FTMT, LOC105379149, 185 more genes
nsv3910959	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 110,798,714-126,528,730 , NCBI36 chr5: 110,826,613-126,556,629 , GRCh38 chr5: 111,463,016-127,193,038	FTMT, LINC02208, 194 more genes
nsv6637111	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 112,557,391-128,106,299 , GRCh38.p12 chr5: 113,221,694-128,770,606	FTMT, SLC12A2, 180 more genes
nsv4456071	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 108,304,806-121,335,239 , GRCh38.p12 chr5: 108,969,105-121,999,544	FTMT, HMGN1P13, 153 more genes
nsv3874025	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 110,407,606-122,522,885 , GRCh38.p12 chr5: 111,071,908-123,187,191	FTMT, LINC02215, 155 more genes
nsv3921962	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 114,707,561-126,507,744 , NCBI36 chr5: 114,071,157-125,871,335 , GRCh37 chr5: 114,043,258-125,843,436	FTMT, RNU2-49P, 139 more genes
nsv3919087	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 120,739,630-126,823,984 , NCBI36 chr5: 120,103,224-126,187,575 , GRCh37 chr5: 120,075,325-126,159,676	FTMT, KRT8P33, 67 more genes
nsv3912909	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 120,031,370-123,861,065 , GRCh38 chr5: 120,695,675-124,525,372 , NCBI36 chr5: 120,059,269-123,888,964	FTMT, SNCAIP, 42 more genes
nsv3886374	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028	FTMT, LOC105374618, 2499 more genes
nsv3871533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343	FTMT, PCDHGC5, 2492 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 31

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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