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Items: 1 to 20 of 103

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5975959insertion1nstd209human GRCh38 chr22: 37,484,416-37,484,416 , GRCh37.p13 chr22: 37,880,454-37,880,454 MFNG
    nsv5669489insertion1nstd207human GRCh38 chr22: 37,484,416-37,484,416 , GRCh37.p13 chr22: 37,880,454-37,880,454 MFNG
    nsv5547837insertion1nstd206human GRCh38 chr22: 37,484,416-37,484,416 , GRCh37.p13 chr22: 37,880,454-37,880,454 MFNG
    nsv5540356copy number variation1nstd206human GRCh38 chr22: 37,464,764-37,469,751 , GRCh37.p13 chr22: 37,860,802-37,865,789 MFNG
    nsv5537833copy number variation1nstd206human GRCh38 chr22: 37,466,372-37,470,997 , GRCh37.p13 chr22: 37,862,410-37,867,035 MFNG
    nsv4757455insertion1nstd199human GRCh37 chr22: 37,880,450-37,880,450 , GRCh38.p12 chr22: 37,484,412-37,484,412 MFNG
    nsv4729926copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824 FBXO7, GTSE1, 1084 more genes
    nsv4721208insertion3nstd186human GRCh37 chr22: 37,880,454-37,880,454 , GRCh38.p12 chr22: 37,484,416-37,484,416 MFNG
    nsv4685545insertion1nstd194human GRCh37 chr22: 37,880,454-37,880,454 , GRCh38.p12 chr22: 37,484,416-37,484,416 MFNG
    nsv4676292copy number variation1nstd102humanPathogenic GRCh37 chr22: 30,654,764-51,197,838 , GRCh38.p12 chr22: 30,258,775-50,759,410 PDXP-DT, PDGFB, 550 more genes
    nsv4564961insertion1nstd166human GRCh37.p13 chr22: 37,880,454-37,880,454 , GRCh38.p12 chr22: 37,484,416-37,484,416 MFNG
    nsv4457771copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,899-51,197,838 , GRCh38.p12 chr22: 16,408,173-50,759,410 IGLV3-27, XKR3, 1082 more genes
    nsv4278013copy number variation1nstd166human GRCh37.p13 chr22: 37,381,892-38,500,309 , GRCh38.p12 chr22: 36,985,851-38,104,302 GGA1, GALR3, 46 more genes
    nsv3961279insertion1nstd168human GRCh38 chr22: 37,455,528-37,470,949 , GRCh37.p13 chr22: 37,851,564-37,866,987 MFNG
    nsv3960679copy number variation1nstd168human GRCh38 chr22: 37,436,070-37,474,127 , GRCh37.p13 chr22: 37,832,105-37,870,165 MFNG
    nsv3922128copy number variation1nstd102humanPathogenic GRCh37 chr22: 35,729,986-39,296,182 , NCBI36 chr22: 34,059,986-37,626,128 , GRCh38 chr22: 35,333,993-38,900,177 LOC102724378, CARD10, 120 more genes
    nsv3919881copy number variation1nstd102humanPathogenic GRCh37 chr22: 17,397,633-51,178,213 , GRCh38 chr22: 16,916,743-50,739,785 , NCBI36 chr22: 15,777,633-49,525,079 MIR12114, MIR6820, 1059 more genes
    nsv3919085copy number variation1nstd102humanPathogenic NCBI36 chr22: 17,008,132-49,591,432 , GRCh37.p13 chr22: 18,628,132-51,244,566 , GRCh38.p12 chr22: 18,145,365-50,806,138 IGLV2-28, LINC01310, 1023 more genes
    nsv3918055copy number variation1nstd102humanUncertain significance GRCh37 chr22: 37,300,872-37,951,517 , NCBI36 chr22: 35,630,818-36,281,463 , GRCh38 chr22: 36,904,830-37,555,510 LOC105373024, ELFN2, 21 more genes
    nsv3917356copy number variation1nstd102humanUncertain significance GRCh37 chr22: 37,520,289-37,976,764 , NCBI36 chr22: 35,850,235-36,306,710 , GRCh38 chr22: 37,124,249-37,580,757 C1QTNF6, LOC105373024, 12 more genes
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