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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143841copy number variation1nstd232human GRCh37.p13 chr2: 157,307,974-157,308,023 , GRCh38.p12 chr2: 156,451,462-156,451,511 GPD2
    nsv7137976copy number variation1nstd232human GRCh37.p13 chr2: 157,347,439-157,347,487 , GRCh38.p12 chr2: 156,490,927-156,490,975 GPD2
    nsv7056410inversion1nstd229human GRCh38 chr2: 155,671,571-160,808,437 , GRCh37.p13 chr2: 156,528,083-161,664,948 LOC105373714, PKP4-AS1, 64 more genes
    nsv7050082inversion1nstd229human GRCh38 chr2: 154,880,025-156,722,310 , GRCh37.p13 chr2: 155,736,537-157,578,822 LOC105373703, LOC107985828, 25 more genes
    nsv7048490inversion1nstd229human GRCh38 chr2: 156,054,444-158,055,095 , GRCh37.p13 chr2: 156,910,956-158,911,607 CYTIP, LINC01876, 23 more genes
    nsv7038090inversion1nstd229human GRCh38 chr2: 152,079,952-160,943,714 , GRCh37.p13 chr2: 152,936,466-161,800,225 , ITGB6, 105 more genes
    nsv6695842copy number variation1nstd229human GRCh38 chr2: 156,518,062-156,521,896 , GRCh37.p13 chr2: 157,374,574-157,378,408 GPD2
    nsv6691606copy number variation1nstd229human GRCh38 chr2: 156,440,316-156,440,419 , GRCh37.p13 chr2: 157,296,828-157,296,931 GPD2
    nsv6689828copy number variation1nstd229human GRCh38 chr2: 156,434,601-156,439,500 , GRCh37.p13 chr2: 157,291,113-157,296,012 GPD2
    nsv6683078copy number variation1nstd229human GRCh38 chr2: 154,503,385-158,170,825 , GRCh37.p13 chr2: 155,359,897-159,027,337 HEBP2P1, RNU6-436P, 48 more genes
    nsv6636792copy number variation1nstd102humanUncertain significance GRCh37 chr2: 156,528,912-158,233,672 , GRCh38.p12 chr2: 155,672,400-157,377,160 RN7SKP281, HEBP2P1, 17 more genes
    nsv6636385copy number variation1nstd102humanLikely pathogenic GRCh38.p12 chr2: 156,139,856-156,515,520 , GRCh37 chr2: 156,996,368-157,372,032 GPD2, NR4A2, 4 more genes
    nsv6551978inversion1nstd223human GRCh38 chr2: 156,491,769-156,492,274 , GRCh37.p13 chr2: 157,348,281-157,348,786 GPD2
    nsv6551440inversion1nstd223human GRCh38 chr2: 156,492,016-156,492,159 , GRCh37.p13 chr2: 157,348,528-157,348,671 GPD2
    nsv6548976inversion1nstd223human GRCh38 chr2: 156,484,372-156,484,561 , GRCh37.p13 chr2: 157,340,884-157,341,073 GPD2
    nsv6352191copy number variation1nstd223human GRCh38 chr2: 156,544,640-156,545,467 , GRCh37.p13 chr2: 157,401,152-157,401,979 GPD2
    nsv6350969copy number variation1nstd223human GRCh38 chr2: 156,553,714-156,554,331 , GRCh37.p13 chr2: 157,410,226-157,410,843 GPD2
    nsv6350576copy number variation1nstd223human GRCh38 chr2: 156,521,962-156,522,169 , GRCh37.p13 chr2: 157,378,474-157,378,681 GPD2
    nsv6346183copy number variation1nstd223human GRCh38 chr2: 156,459,429-156,466,621 , GRCh37.p13 chr2: 157,315,941-157,323,133 GPD2
    nsv6345646copy number variation1nstd223human GRCh38 chr2: 156,512,565-156,513,200 , GRCh37.p13 chr2: 157,369,077-157,369,712 GPD2
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