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Items: 1 to 20 of 299

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076339inversion1nstd229human GRCh38 chr16: 70,122,272-74,889,687 , GRCh37.p13 chr16: 70,156,175-74,923,585 SNORD111B, HCCAT5, 96 more genes
    nsv7071664inversion1nstd229human GRCh38 chr16: 70,115,686-74,569,766 , GRCh37.p13 chr16: 70,149,589-74,603,664 RPL21P118, GLG1, 89 more genes
    nsv7069342inversion1nstd229human GRCh38 chr16: 70,164,048-74,471,145 , GRCh37.p13 chr16: 70,197,951-74,505,043 GLG1, RPL21P118, 88 more genes
    nsv7066185inversion1nstd229human GRCh38 chr16: 71,798,581-75,423,466 , GRCh37.p13 chr16: 71,832,484-75,457,364 TMPOP2, RPSAP56, 57 more genes
    nsv7064268inversion1nstd229human GRCh38 chr16: 69,686,669-74,423,188 , GRCh37.p13 chr16: 69,720,572-74,457,086 LOC102723786, RNU7-90P, 99 more genes
    nsv7061930inversion1nstd229human GRCh38 chr16: 71,759,694-75,426,750 , GRCh37.p13 chr16: 71,793,597-75,460,648 BCAR1, LOC105371343, 57 more genes
    nsv7058675inversion1nstd229human GRCh38 chr16: 67,667,666-75,720,241 , GRCh37.p13 chr16: 67,701,569-75,754,139 RNU6-898P, DPEP2, 199 more genes
    nsv6990105copy number variation1nstd229human GRCh38 chr16: 73,750,281-74,500,796 , GRCh37.p13 chr16: 73,784,180-74,534,694 PDPR2P, RPSAP56, 14 more genes
    nsv6989370copy number variation1nstd229human GRCh38 chr16: 74,329,552-74,472,529 , GRCh37.p13 chr16: 74,363,450-74,506,427 NPIPB15, LOC105376772, 5 more genes
    nsv6983408copy number variation1nstd229human GRCh38 chr16: 74,048,861-75,393,024 , GRCh37.p13 chr16: 74,082,760-75,426,922 PSMD7, RNU6-237P, 28 more genes
    nsv6637595copy number variation1nstd102humanUncertain significance GRCh37 chr16: 73,673,334-78,137,887 , GRCh38.p12 chr16: 73,639,435-78,103,990 CNTNAP4, WDR59, 73 more genes
    nsv6637493copy number variation1nstd102humanUncertain significance GRCh37 chr16: 73,673,334-76,105,189 , GRCh38.p12 chr16: 73,639,435-76,071,291 LOC105371347, LOC105371344, 51 more genes
    nsv6637273copy number variation1nstd102humanUncertain significance GRCh37 chr16: 73,858,079-75,855,162 , GRCh38.p12 chr16: 73,824,180-75,821,264 LOC105371344, CTRB2, 46 more genes
    nsv6634465copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 71,610,276-90,354,753 , GRCh38.p12 chr16: 71,576,373-90,228,345 AP1G1, AFG3L1P, 349 more genes
    nsv6511987copy number variation1nstd223human GRCh38 chr16: 74,351,401-74,465,200 , GRCh37.p13 chr16: 74,385,299-74,499,098 GLG1, CLEC18B, 5 more genes
    nsv6508066copy number variation1nstd223human GRCh38 chr16: 74,417,701-74,427,800 , GRCh37.p13 chr16: 74,451,599-74,461,698 CLEC18B, LOC107984827
    nsv6505432copy number variation1nstd223human GRCh38 chr16: 74,386,228-74,437,809 , GRCh37.p13 chr16: 74,420,126-74,471,707 NPIPB15, CLEC18B, 2 more genes
    nsv6503615copy number variation1nstd223human GRCh38 chr16: 73,789,935-74,447,058 , GRCh37.p13 chr16: 73,823,834-74,480,956 PDPR2P, RPSAP56, 12 more genes
    nsv6502068copy number variation1nstd223human GRCh38 chr16: 74,352,901-74,428,600 , GRCh37.p13 chr16: 74,386,799-74,462,498 LOC105376772, LOC107984827, 3 more genes
    nsv6499975copy number variation1nstd223human GRCh38 chr16: 74,414,120-74,440,912 , GRCh37.p13 chr16: 74,448,018-74,474,810 LOC107984827, CLEC18B
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