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Items: 1 to 20 of 152

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5426312copy number variation1nstd206human GRCh38 chr1: 158,844,018-158,853,440 , GRCh37.p13 chr1: 158,813,808-158,823,230 MNDA
    nsv5424937copy number variation1nstd206human GRCh38 chr1: 158,837,837-158,839,052 , GRCh37.p13 chr1: 158,807,627-158,808,842 OR6N1, MNDA
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5212339copy number variation1nstd204human GRCh38.p13 chr1: 158,835,001-158,838,900 , GRCh37.p13 chr1: 158,804,791-158,808,690 MNDA, OR6N1
    nsv4897682copy number variation1nstd200human GRCh38 chr1: 158,844,018-158,853,440 , GRCh37.p13 chr1: 158,813,808-158,823,230 MNDA
    nsv4897681copy number variation1nstd200human GRCh38 chr1: 158,837,837-158,839,052 , GRCh37.p13 chr1: 158,807,627-158,808,842 MNDA, OR6N1
    nsv4897680copy number variation1nstd200human GRCh38 chr1: 158,837,111-158,838,396 , GRCh37.p13 chr1: 158,806,901-158,808,186 OR6N1, MNDA
    nsv4897674copy number variation1nstd200human GRCh38 chr1: 158,711,214-158,879,715 , GRCh37.p13 chr1: 158,681,004-158,849,505 OR6K4P, PYHIN5P, 8 more genes
    nsv4784402copy number variation1nstd200human GRCh37 chr1: 158,813,808-158,823,230 , GRCh38.p12 chr1: 158,844,018-158,853,440 MNDA
    nsv4784401copy number variation1nstd200human GRCh37 chr1: 158,807,627-158,808,842 , GRCh38.p12 chr1: 158,837,837-158,839,052 MNDA, OR6N1
    nsv4784396copy number variation1nstd200human GRCh37 chr1: 158,681,004-158,849,505 , GRCh38.p12 chr1: 158,711,214-158,879,715 MNDA, OR6K5P, 8 more genes
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4674553copy number variation1nstd102humanUncertain significance GRCh37 chr1: 158,489,545-158,889,411 , GRCh38.p12 chr1: 158,519,755-158,919,621 OR6K2, OR6N2, 16 more genes
    nsv4579499copy number variation1nstd183human GRCh37 chr1: 158,711,658-158,972,043 , GRCh38.p12 chr1: 158,741,868-159,002,253 PYDC5, OR2AQ1P, 9 more genes
    nsv4579399copy number variation1nstd183human GRCh37 chr1: 158,813,807-158,823,230 , GRCh38.p12 chr1: 158,844,017-158,853,440 MNDA
    nsv4570495mobile element insertion1nstd166human GRCh37.p13 chr1: 158,816,004-158,816,004 , GRCh38.p12 chr1: 158,846,214-158,846,214 MNDA
    nsv4458970mobile element insertion1nstd166human GRCh37.p13 chr1: 158,809,038-158,809,038 , GRCh38.p12 chr1: 158,839,248-158,839,248 MNDA, OR6N1
    nsv4450412copy number variation1nstd102humanPathogenic GRCh37 chr1: 157,321,299-167,391,423 , GRCh38.p12 chr1: 157,351,509-167,422,186 FCGR3B, SLAMF9, 302 more genes
    nsv4385444copy number variation1nstd173human GRCh37 chr1: 158,214,469-159,706,408 , GRCh38.p12 chr1: 158,244,679-159,736,618 , RAD1P2, 60 more genes
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