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Items: 1 to 20 of 442

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144759copy number variation1nstd232human GRCh37.p13 chr5: 131,120,702-131,120,771 , GRCh38.p12 chr5: 131,785,009-131,785,078 FNIP1
    nsv7140492copy number variation1nstd232human GRCh37.p13 chr5: 131,120,743-131,120,838 , GRCh38.p12 chr5: 131,785,050-131,785,145 FNIP1
    nsv7137085copy number variation1nstd102humanPathogenic GRCh37 chr5: 127,800,418-134,002,686 , GRCh38.p12 chr5: 128,464,725-134,666,996 CSF2, LOC402229, 99 more genes
    nsv7098986copy number variation1nstd102humanPathogenic GRCh37 chr5: 130,766,131-131,044,893 , GRCh38.p12 chr5: 131,430,438-131,709,200 FNIP1, RAPGEF6, 1 more genes
    nsv7050047inversion1nstd229human GRCh38 chr5: 126,094,727-134,977,523 , GRCh37.p13 chr5: 125,430,420-134,313,213 RNU6-757P, SKP1, 145 more genes
    nsv7044234inversion1nstd229human GRCh38 chr5: 125,118,269-132,850,844 , GRCh37.p13 chr5: 124,453,962-132,186,536 RPLP1P7, IL4, 98 more genes
    nsv7042985inversion1nstd229human GRCh38 chr5: 129,885,016-134,639,437 , GRCh37.p13 chr5: 129,220,709-133,975,127 HSPA8P4, LINC02999, 85 more genes
    nsv7042749inversion1nstd229human GRCh38 chr5: 125,171,898-132,850,836 , GRCh37.p13 chr5: 124,507,591-132,186,528 LOC102723654, LOC105379174, 98 more genes
    nsv6797785copy number variation1nstd229human GRCh38 chr5: 131,724,773-131,724,801 , GRCh37.p13 chr5: 131,060,466-131,060,494 FNIP1
    nsv6795365copy number variation1nstd229human GRCh38 chr5: 131,786,437-131,787,098 , GRCh37.p13 chr5: 131,122,130-131,122,791 FNIP1
    nsv6792860copy number variation1nstd229human GRCh38 chr5: 131,773,571-131,778,224 , GRCh37.p13 chr5: 131,109,264-131,113,917 FNIP1
    nsv6792137copy number variation1nstd229human GRCh38 chr5: 131,671,101-131,691,500 , GRCh37.p13 chr5: 131,006,794-131,027,193 FNIP1
    nsv6791827copy number variation1nstd229human GRCh38 chr5: 131,682,401-131,687,600 , GRCh37.p13 chr5: 131,018,094-131,023,293 FNIP1
    nsv6791500copy number variation1nstd229human GRCh38 chr5: 131,697,683-131,746,854 , GRCh37.p13 chr5: 131,033,376-131,082,547 FNIP1
    nsv6790182copy number variation1nstd229human GRCh38 chr5: 131,697,382-131,929,694 , GRCh37.p13 chr5: 131,033,075-131,265,387 MEIKIN, FNIP1
    nsv6789924copy number variation1nstd229human GRCh38 chr5: 131,709,292-131,709,458 , GRCh37.p13 chr5: 131,044,985-131,045,151 FNIP1
    nsv6787056copy number variation1nstd229human GRCh38 chr5: 126,804,198-136,494,917 , GRCh37.p13 chr5: 126,139,890-135,830,606 SLC22A4, LOC105379199, 158 more genes
    nsv6786090copy number variation1nstd229human GRCh38 chr5: 131,712,248-131,712,326 , GRCh37.p13 chr5: 131,047,941-131,048,019 FNIP1
    nsv6784682copy number variation1nstd229human GRCh38 chr5: 131,640,227-131,643,450 , GRCh37.p13 chr5: 130,975,920-130,979,143 FNIP1
    nsv6784222copy number variation1nstd229human GRCh38 chr5: 131,754,437-131,785,995 , GRCh37.p13 chr5: 131,090,130-131,121,688 FNIP1
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