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Items: 1 to 20 of 114

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093376copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 156,786,013-162,945,369 , GRCh38.p12 chr5: 157,359,005-163,518,363 ADRA1B, CCNG1, 81 more genes
    nsv7055491inversion1nstd229human GRCh38 chr5: 157,701,805-157,831,931 , GRCh37.p13 chr5: 157,128,813-157,258,939 RNU6-260P, THG1L, 3 more genes
    nsv7052590inversion1nstd229human GRCh38 chr5: 154,695,187-159,271,728 , GRCh37.p13 chr5: 154,074,747-158,698,736 MRPL22, LOC105377673, 58 more genes
    nsv6794325copy number variation1nstd229human GRCh38 chr5: 157,712,920-157,761,553 , GRCh37.p13 chr5: 157,139,928-157,188,561 THG1L, LSM11
    nsv6792298copy number variation1nstd229human GRCh38 chr5: 157,736,699-157,736,903 , GRCh37.p13 chr5: 157,163,707-157,163,911 THG1L
    nsv6783218copy number variation1nstd229human GRCh38 chr5: 157,626,001-157,758,800 , GRCh37.p13 chr5: 157,053,009-157,185,808 THG1L, LSM11, 5 more genes
    nsv6779551copy number variation1nstd229human GRCh38 chr5: 157,740,436-157,743,289 , GRCh37.p13 chr5: 157,167,444-157,170,297 LSM11, THG1L
    nsv6636891copy number variation1nstd102humanPathogenic GRCh37 chr5: 150,535,183-172,906,793 , GRCh38.p12 chr5: 151,155,622-173,479,790 EFCAB9, LOC112267936, 287 more genes
    nsv6566032inversion1nstd223human GRCh38 chr5: 157,740,732-157,741,846 , GRCh37.p13 chr5: 157,167,740-157,168,854 LSM11, THG1L
    nsv6564783inversion1nstd223human GRCh38 chr5: 157,734,396-157,734,947 , GRCh37.p13 chr5: 157,161,404-157,161,955 THG1L
    nsv6315448copy number variation1nstd102humanPathogenic GRCh37 chr5: 149,010,383-180,719,789 , GRCh38.p12 chr5: 149,630,820-181,292,788 GRM6, MIR1229, 554 more genes
    nsv6290966copy number variation1nstd102humannot provided GRCh37 chr5: 155,970,607-162,450,579 , GRCh38.p12 chr5: 156,543,597-163,023,573 C1QTNF2, MED7, 86 more genes
    nsv6135388copy number variation1nstd213human GRCh37 chr5: 153,010,000-160,030,001 , GRCh38.p12 chr5: 153,630,440-160,602,994 ADRA1B, EBF1, 107 more genes
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4674945copy number variation1nstd102humanPathogenic GRCh37 chr5: 156,347,980-169,959,880 , GRCh38.p12 chr5: 156,920,969-170,532,876 LINC02227, LINC01932, 146 more genes
    nsv4455586copy number variation1nstd102humanPathogenic GRCh37 chr5: 156,597,181-171,166,353 , GRCh38.p12 chr5: 157,170,170-171,739,349 LOC105377677, GABRA6, 164 more genes
    nsv4342767sequence alteration1nstd166human GRCh37.p13 chr5: 157,153,905-157,170,414 , GRCh38.p12 chr5: 157,726,897-157,743,406 THG1L, LSM11
    nsv4113309copy number variation1nstd166human GRCh37.p13 chr5: 157,162,009-157,203,001 , GRCh38.p12 chr5: 157,735,001-157,775,993 LSM11, THG1L
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