fnip1[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
nsv3875298	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 131,044,312-131,127,575 , GRCh38.p12 chr5: 131,708,619-131,791,882	FNIP1
nsv6290733	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 131,025,250-131,232,887 , GRCh38.p12 chr5: 131,689,557-131,897,194	FNIP1, MEIKIN
nsv3921295	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr5: 131,065,248-131,246,969 , GRCh37 chr5: 131,037,349-131,219,070 , GRCh38 chr5: 131,701,656-131,883,377	FNIP1, MEIKIN
nsv7098986	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 130,766,131-131,044,893 , GRCh38.p12 chr5: 131,430,438-131,709,200	FNIP1, RAPGEF6, 1 more genes
nsv4455997	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 130,764,058-131,206,406 , GRCh38.p12 chr5: 131,428,365-131,870,713	FNIP1, MEIKIN, 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	FNIP1, 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	FNIP1, 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	FNIP1, LINC01023, 783 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	FNIP1, LOC105379149, 185 more genes
nsv3920627	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 126,864,591-135,314,282 , GRCh37.p13 chr5: 126,836,692-135,286,383 , GRCh38.p12 chr5: 127,501,000-135,950,694	FNIP1, MIR1289-2, 138 more genes
nsv3911932	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 125,774,098-132,209,659 , NCBI36 chr5: 125,801,997-132,237,558 , GRCh38 chr5: 126,438,406-132,873,967	FNIP1, LOC105379176, 93 more genes
nsv7137085	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 127,800,418-134,002,686 , GRCh38.p12 chr5: 128,464,725-134,666,996	FNIP1, CSF2, 99 more genes
nsv3916850	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 130,962,196-135,150,743 , NCBI36 chr5: 130,990,095-135,178,642 , GRCh38 chr5: 131,626,503-135,815,054	FNIP1, SLC25A48-AS1, 96 more genes
nsv4681617	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 130,497,712-131,729,974 , GRCh38.p12 chr5: 131,162,019-132,394,282	FNIP1, MIR6830, 19 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	FNIP1, 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	FNIP1, PCDHGC5, 2492 more genes
nsv3875235	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788	FNIP1, SPEF2, 2490 more genes
nsv3874238	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 106,716,357-180,687,338 , GRCh38.p12 chr5: 107,380,656-181,260,337	FNIP1, PJA2, 1228 more genes
nsv3878636	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 130,125,085-157,574,910 , GRCh38.p12 chr5: 130,789,392-158,147,902	FNIP1, LOC100288484, 551 more genes
nsv3923414	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 130,196,621-154,701,371 , NCBI36 chr5: 130,224,520-154,681,564 , GRCh38 chr5: 130,860,928-155,321,811	FNIP1, HNRNPA3P7, 514 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 27

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Number of Variants: 20

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Supplemental Content

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Search details

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