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Items: 1 to 20 of 126

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7056347inversion1nstd229human GRCh38 chr5: 86,534,141-86,719,672 , GRCh37.p13 chr5: 85,829,958-86,015,489 RNU6-804P, SNORD138, 1 more genes
    nsv7054901inversion1nstd229human GRCh38 chr5: 86,506,255-87,299,369 , GRCh37.p13 chr5: 85,802,072-86,595,186 RN7SL629P, MIR4280, 12 more genes
    nsv7053596inversion1nstd229human GRCh38 chr5: 85,730,857-88,063,519 , GRCh37.p13 chr5: 85,026,675-87,359,336 LOC100421863, RPL10AP9, 25 more genes
    nsv7050687inversion1nstd229human GRCh38 chr5: 86,603,498-87,299,362 , GRCh37.p13 chr5: 85,899,315-86,595,179 RPL10AP9, LINC01949, 12 more genes
    nsv7045583inversion1nstd229human GRCh38 chr5: 86,305,164-86,775,367 , GRCh37.p13 chr5: 85,600,982-86,071,184 LINC02059, LOC105379064, 4 more genes
    nsv7042170inversion1nstd229human GRCh38 chr5: 86,596,140-86,616,492 , GRCh37.p13 chr5: 85,891,957-85,912,309 COX7C
    nsv6773991copy number variation1nstd229human GRCh38 chr5: 86,610,196-86,645,309 , GRCh37.p13 chr5: 85,906,013-85,941,126 COX7C, SNORD138
    nsv6769416copy number variation1nstd229human GRCh38 chr5: 86,608,887-86,629,260 , GRCh37.p13 chr5: 85,904,704-85,925,077 SNORD138, COX7C
    nsv6763486copy number variation1nstd229human GRCh38 chr5: 86,611,979-86,657,106 , GRCh37.p13 chr5: 85,907,796-85,952,923 COX7C, SNORD138
    nsv6760412copy number variation1nstd229human GRCh38 chr5: 86,127,035-87,005,434 , GRCh37.p13 chr5: 85,422,853-86,301,251 COX7C, LOC100421863, 6 more genes
    nsv6636247copy number variation1nstd102humanUncertain significance GRCh37 chr5: 85,849,576-86,109,647 , GRCh38.p12 chr5: 86,553,759-86,813,830 LINC02059, RNU6-804P, 2 more genes
    nsv6398739copy number variation1nstd223human GRCh38 chr5: 83,701,679-87,055,970 , GRCh37.p13 chr5: 82,997,498-86,351,787 LOC645261, LOC105379061, 28 more genes
    nsv6313788copy number variation1nstd102humanPathogenic GRCh37 chr5: 82,185,951-90,110,454 , GRCh38.p12 chr5: 82,890,132-90,814,637 RASA1, HAPLN1, 82 more genes
    nsv6136135copy number variation1nstd213human GRCh37 chr5: 85,890,000-86,050,001 , GRCh38.p12 chr5: 86,594,183-86,754,184 COX7C, LINC02059, 2 more genes
    nsv6135438copy number variation1nstd213human GRCh37 chr5: 80,920,000-86,370,001 , GRCh38.p12 chr5: 81,624,181-87,074,184 COX7C, HAPLN1, 56 more genes
    nsv6135436copy number variation1nstd213human GRCh37 chr5: 70,260,000-91,630,001 , GRCh38.p12 chr5: 70,964,173-92,334,184 , ARSB, 300 more genes
    nsv6135200copy number variation1nstd213human GRCh37 chr5: 76,540,000-94,260,001 , GRCh38.p12 chr5: 77,244,175-94,924,296 ACTBP2, ARSB, 200 more genes
    nsv5687116mobile element insertion2nstd211human GRCh38 chr5: 86,616,770-86,616,770 , GRCh37.p13 chr5: 85,912,587-85,912,587 COX7C
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv5033775inversion1nstd200human GRCh38 chr5: 76,373,686-102,541,075 , GRCh37.p13 chr5: 75,669,511-101,876,779 , F2RL1, 331 more genes
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