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Items: 1 to 20 of 262

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094940copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,611,036-90,106,937 , GRCh38.p12 chr16: 89,544,628-90,040,529 SPATA2L, LINC02166, 25 more genes
    nsv7094699copy number variation2nstd102humanUncertain significance GRCh37 chr16: 87,636,753-90,109,753 , GRCh38.p12 chr16: 87,603,147-90,043,345 HSALR1, LOC105371412, 87 more genes
    nsv6990538copy number variation1nstd229human GRCh38 chr16: 89,924,595-89,924,643 , GRCh37.p13 chr16: 89,991,003-89,991,051 TUBB3
    nsv6990193copy number variation1nstd229human GRCh38 chr16: 89,932,079-89,932,144 , GRCh37.p13 chr16: 89,998,487-89,998,552 TUBB3
    nsv6988771copy number variation1nstd229human GRCh38 chr16: 89,924,685-89,936,027 , GRCh37.p13 chr16: 89,991,093-90,002,435 TUBB3
    nsv6981818copy number variation1nstd229human GRCh38 chr16: 89,916,901-89,921,100 , GRCh37.p13 chr16: 89,983,309-89,987,508 MC1R, TUBB3
    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
    nsv6515307copy number variation1nstd223human GRCh38 chr16: 89,932,711-89,933,161 , GRCh37.p13 chr16: 89,999,119-89,999,569 TUBB3
    nsv6500661copy number variation1nstd223human GRCh38 chr16: 89,839,303-90,017,373 , GRCh37.p13 chr16: 89,905,711-90,083,781 DEF8, SPIRE2, 8 more genes
    nsv6499720copy number variation1nstd223human GRCh38 chr16: 89,919,798-89,920,802 , GRCh37.p13 chr16: 89,986,206-89,987,210 TUBB3, MC1R
    nsv6496750copy number variation1nstd223human GRCh38 chr16: 89,926,887-89,928,650 , GRCh37.p13 chr16: 89,993,295-89,995,058 TUBB3
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6291643copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,337,891-90,155,062 , GRCh38.p12 chr16: 89,271,483-90,088,654 DBNDD1, AFG3L1P, 34 more genes
    nsv6291569copy number variation1nstd102humanUncertain significance GRCh37 chr16: 88,000,389-90,155,062 , GRCh38.p12 chr16: 87,966,783-90,088,654 CTU2, CDT1, 78 more genes
    nsv6290331copy number variation1nstd102humanPathogenic GRCh37 chr16: 80,386,595-90,163,348 , GRCh38.p12 chr16: 80,352,698-90,096,940 GINS2, TCF25, 220 more genes
    nsv6275023copy number variation1nstd214human GRCh38 chr16: 89,934,127-89,934,208 , GRCh37.p13 chr16: 90,000,535-90,000,616 TUBB3
    nsv6274319copy number variation1nstd214human GRCh38 chr16: 89,933,939-89,934,020 , GRCh37.p13 chr16: 90,000,347-90,000,428 TUBB3
    nsv6196007copy number variation1nstd214human GRCh38 chr16: 89,932,079-89,932,143 , GRCh37.p13 chr16: 89,998,487-89,998,551 TUBB3
    nsv6133287copy number variation1nstd213human GRCh37 chr16: 88,280,000-90,210,001 , GRCh38.p12 chr16: 88,246,394-90,143,593 AFG3L1P, APRT, 79 more genes
    nsv6133217copy number variation1nstd213human GRCh37 chr16: 89,240,000-90,180,001 , GRCh38.p12 chr16: 89,173,592-90,113,593 AFG3L1P, GAS8-AS1, 40 more genes
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