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Items: 1 to 20 of 230

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5950849insertion1nstd209human GRCh38 chr5: 7,864,812-7,864,812 , GRCh37.p13 chr5: 7,864,925-7,864,925 MTRR, FASTKD3
    nsv5686612mobile element insertion2nstd211human GRCh38 chr5: 7,864,822-7,864,822 , GRCh37.p13 chr5: 7,864,935-7,864,935 FASTKD3, MTRR
    nsv5627548insertion1nstd207human GRCh38 chr5: 7,864,812-7,864,812 , GRCh37.p13 chr5: 7,864,925-7,864,925 MTRR, FASTKD3
    nsv5473082copy number variation1nstd206human GRCh38 chr5: 7,798,999-8,835,000 , GRCh37.p13 chr5: 7,799,112-8,835,112 ADCY2, LOC102723339, 13 more genes
    nsv5400049mobile element insertion1nstd206human GRCh38 chr5: 7,864,822-7,864,873 , GRCh37.p13 chr5: 7,864,935-7,864,986 FASTKD3, MTRR
    nsv5381771copy number variation1nstd102humanPathogenic GRCh37 chr5: 22,149-29,048,823 , GRCh38.p12 chr5: 22,149-29,048,716 OTULINL, AKTIPP2, 317 more genes
    nsv5085503mobile element insertion1nstd203human GRCh38 chr5: 7,864,812-7,864,822 , GRCh37.p13 chr5: 7,864,925-7,864,935 FASTKD3, MTRR
    nsv5084087mobile element insertion1nstd203human GRCh38 chr5: 7,864,816-7,864,822 , GRCh37.p13 chr5: 7,864,929-7,864,935 FASTKD3, MTRR
    nsv5041416inversion1nstd200human GRCh38 chr5: 6,583,518-8,812,732 , GRCh37.p13 chr5: 6,583,631-8,812,844 RNA5SP176, MTND6P2, 36 more genes
    nsv4729582copy number variation1nstd102humanLikely benign GRCh37 chr5: 7,619,352-8,166,508 , GRCh38.p12 chr5: 7,619,239-8,166,395 CFAP90, LOC100422730, 5 more genes
    nsv4725726insertion1nstd186human GRCh37 chr5: 7,864,925-7,864,925 , GRCh38.p12 chr5: 7,864,812-7,864,812 MTRR, FASTKD3
    nsv4686906mobile element insertion1nstd186human GRCh37 chr5: 7,864,939-7,864,939 , GRCh38.p12 chr5: 7,864,826-7,864,826 MTRR, FASTKD3
    nsv4685752copy number variation1nstd102humanPathogenic GRCh37 chr5: 71,904-22,078,969 , GRCh38.p12 chr5: 71,789-22,078,860 LINC01377, LOC100421308, 277 more genes
    nsv4682276copy number variation1nstd102humanPathogenic GRCh37 chr5: 7,869,227-7,900,191 , GRCh38.p12 chr5: 7,869,114-7,900,078 FASTKD3, MTRR
    nsv4674497copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-14,738,180 , GRCh38.p12 chr5: 113,461-14,738,071 LOC101929003, MTCYBP37, 192 more genes
    nsv4674444copy number variation1nstd102humanPathogenic GRCh37 chr5: 1,322,680-10,762,544 , GRCh38.p12 chr5: 1,322,565-10,762,432 LOC100132773, LINC01019, 125 more genes
    nsv4674418copy number variation1nstd102humanUncertain significance GRCh37 chr5: 7,263,294-8,372,692 , GRCh38.p12 chr5: 7,263,181-8,372,579 RNU1-76P, MTRR, 15 more genes
    nsv4674161copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-23,364,376 , GRCh38.p12 chr5: 113,461-23,364,267 LOC102723561, LOC107986397, 287 more genes
    nsv4674130copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-11,767,720 , GRCh38.p12 chr5: 113,461-11,767,608 SLC9A3-AS1, LINC02114, 169 more genes
    nsv4598280copy number variation1nstd183human GRCh37 chr5: 7,862,443-8,081,049 , GRCh38.p12 chr5: 7,862,330-8,080,936 MTRR, RNU1-76P, 3 more genes
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