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Items: 1 to 20 of 38

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3913013copy number variation1nstd102humanPathogenic GRCh38 chr17: 162,016-7,697,012 , GRCh37 chr17: 45,835-7,600,330 , NCBI36 chr17: 11,807-7,541,055 YBX2, 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 YBX2, 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 YBX2, 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 YBX2, CTC1, 103 more genes
    nsv6314103copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,020,054-8,086,290 , GRCh38.p12 chr17: 7,116,735-8,182,972 YBX2, RPL7AP64, 87 more genes
    nsv7094915copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,120,455-8,151,423 , GRCh38.p12 chr17: 7,217,136-8,248,105 YBX2, 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 YBX2, FXR2, 76 more genes
    nsv7098895copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,004,894-7,766,789 , GRCh38.p12 chr17: 7,101,575-7,863,471 YBX2, LOC105371512, 61 more genes
    nsv4676022copy number variation1nstd102humanPathogenic GRCh37 chr17: 6,800,893-7,304,696 , GRCh38.p12 chr17: 6,897,574-7,401,377 YBX2, 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 YBX2, DVL2, 29 more genes
    nsv4729957copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,014,481-7,283,233 , GRCh38.p12 chr17: 7,111,162-7,379,914 YBX2, 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 YBX2, 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 YBX2, ASGR1, 11 more genes
    nsv3903684copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004 YBX2, MIR3185, 2366 more genes
    nsv3899740copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564 YBX2, P4HB, 2366 more genes
    nsv3906245copy number variation1nstd102humanPathogenic GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251 YBX2, MIR21, 2366 more genes
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 YBX2, SMURF2, 2366 more genes
    nsv3897625copy number variation1nstd102humanPathogenic GRCh37 chr17: 525-15,027,737 , GRCh38.p12 chr17: 150,732-15,124,420 YBX2, GP1BA, 439 more genes
    nsv3915354copy number variation1nstd102humanPathogenic GRCh38 chr17: 150,732-14,764,202 , NCBI36 chr17: 525-14,608,244 , GRCh37 chr17: 525-14,667,519 YBX2, KIF1C-AS1, 433 more genes
    nsv3917059copy number variation1nstd102humanPathogenic GRCh37 chr17: 45,835-12,247,218 , NCBI36 chr17: 11,807-12,187,943 , GRCh38 chr17: 162,016-12,343,901 YBX2, PSMB6, 409 more genes
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