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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095364copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,126,433-7,126,544 , GRCh38.p12 chr17: 7,223,114-7,223,225 ACADVL, MIR324
    nsv5673024copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 7,125,898-7,126,003 , GRCh38 chr17: 7,222,579-7,222,684 ACADVL, MIR324
    nsv7095415copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,124,120-7,128,078 , GRCh38.p12 chr17: 7,220,801-7,224,759 ACADVL, DVL2, 1 more genes
    nsv3913013copy number variation1nstd102humanPathogenic GRCh38 chr17: 162,016-7,697,012 , GRCh37 chr17: 45,835-7,600,330 , NCBI36 chr17: 11,807-7,541,055 ACADVL, RPS4XP17, 289 more genes
    nsv3910343copy number variation1nstd102humanPathogenic GRCh37 chr17: 5,636,297-7,942,140 , NCBI36 chr17: 5,577,021-7,882,865 , GRCh38 chr17: 5,732,977-8,038,822 ACADVL, RPL23AP73, 106 more genes
    nsv1397967copy number variation1nstd102humanPathogenic NCBI36 chr17: 6,838,295-7,991,364 , GRCh37.p13 chr17: 6,897,571-8,050,639 , GRCh38.p12 chr17: 6,994,252-8,147,321 ACADVL, TNFSF12-TNFSF13, 96 more genes
    nsv7095414copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,123,304-8,193,254 , GRCh38.p12 chr17: 7,219,985-8,289,936 ACADVL, CTC1, 103 more genes
    nsv6314103copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,020,054-8,086,290 , GRCh38.p12 chr17: 7,116,735-8,182,972 ACADVL, RPL7AP64, 87 more genes
    nsv7094915copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,120,455-8,151,423 , GRCh38.p12 chr17: 7,217,136-8,248,105 ACADVL, MIR324, 101 more genes
    nsv1398205copy number variation1nstd102humanPathogenic NCBI36 chr17: 7,033,635-7,977,678 , GRCh37.p13 chr17: 7,092,911-8,036,953 , GRCh38.p12 chr17: 7,189,592-8,133,635 ACADVL, YBX2, 76 more genes
    nsv7098895copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,004,894-7,766,789 , GRCh38.p12 chr17: 7,101,575-7,863,471 ACADVL, LOC105371512, 61 more genes
    nsv5673052copy number variation1nstd102humanPathogenic GRCh37 chr17: 6,589,506-7,128,436 , GRCh38.p12 chr17: 6,686,187-7,225,117 ACADVL, RPL23AP73, 25 more genes
    nsv4676022copy number variation1nstd102humanPathogenic GRCh37 chr17: 6,800,893-7,304,696 , GRCh38.p12 chr17: 6,897,574-7,401,377 ACADVL, DVL2, 37 more genes
    nsv3922376copy number variation1nstd102humanPathogenic GRCh38 chr17: 7,210,345-7,496,934 , NCBI36 chr17: 7,054,388-7,340,977 , GRCh37 chr17: 7,113,664-7,400,253 ACADVL, DVL2, 29 more genes
    nsv4729957copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,014,481-7,283,233 , GRCh38.p12 chr17: 7,111,162-7,379,914 ACADVL, MIR324, 20 more genes
    nsv1398520copy number variation1nstd102humanPathogenic NCBI36 chr17: 6,936,148-7,177,360 , GRCh37.p13 chr17: 6,995,424-7,236,636 , GRCh38.p12 chr17: 7,092,105-7,333,317 ACADVL, EIF5A, 16 more genes
    nsv1398446copy number variation1nstd102humanPathogenic NCBI36 chr17: 6,996,378-7,152,828 , GRCh37.p13 chr17: 7,055,654-7,212,104 , GRCh38.p12 chr17: 7,152,335-7,308,785 ACADVL, ASGR1, 11 more genes
    nsv3903684copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004 ACADVL, MIR3185, 2366 more genes
    nsv3899740copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564 ACADVL, P4HB, 2366 more genes
    nsv3906245copy number variation1nstd102humanPathogenic GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251 ACADVL, MIR21, 2366 more genes
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