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Items: 1 to 20 of 251

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099244copy number variation1nstd231human GRCh38.p12 chr1: 166,864,890-169,028,321 , GRCh37 chr1: 166,834,127-168,997,559 CD247, DPT, 49 more genes
    nsv7054284inversion1nstd229human GRCh38 chr1: 168,606,664-168,716,677 , GRCh37.p13 chr1: 168,575,902-168,685,915 LOC105371604, DPT
    nsv6644271copy number variation1nstd229human GRCh38 chr1: 168,628,156-168,820,156 , GRCh37.p13 chr1: 168,597,394-168,789,394 LOC105371604, LINC00626, 1 more genes
    nsv6644256copy number variation1nstd229human GRCh38 chr1: 168,110,598-170,953,728 , GRCh37.p13 chr1: 168,079,836-170,922,869 SELL, RPL7AP21, 55 more genes
    nsv6644163copy number variation1nstd229human GRCh38 chr1: 168,725,001-168,750,800 , GRCh37.p13 chr1: 168,694,239-168,720,038 DPT
    nsv6644161copy number variation1nstd229human GRCh38 chr1: 168,658,534-168,788,448 , GRCh37.p13 chr1: 168,627,772-168,757,686 DPT, LOC105371604, 1 more genes
    nsv6643780copy number variation1nstd229human GRCh38 chr1: 168,671,300-168,697,470 , GRCh37.p13 chr1: 168,640,538-168,666,708 DPT
    nsv6637036copy number variation1nstd102humanUncertain significance GRCh37 chr1: 168,675,820-169,363,333 , GRCh38.p12 chr1: 168,706,582-169,394,095 LOC101928596, CCDC181, 10 more genes
    nsv6540250inversion1nstd223human GRCh38 chr1: 163,441,141-169,028,378 , GRCh37.p13 chr1: 163,410,931-168,997,616 LOC107985452, NMNAT1P2, 96 more genes
    nsv6331627copy number variation1nstd223human GRCh38 chr1: 168,671,300-168,697,468 , GRCh37.p13 chr1: 168,640,538-168,666,706 DPT
    nsv6331329copy number variation1nstd223human GRCh38 chr1: 168,698,864-168,699,850 , GRCh37.p13 chr1: 168,668,102-168,669,088 DPT
    nsv6313719copy number variation1nstd102humanPathogenic GRCh37 chr1: 162,330,810-171,532,331 , GRCh38.p12 chr1: 162,361,020-171,563,192 LOC100420658, LOC105371610, 167 more genes
    nsv6313602copy number variation1nstd102humanPathogenic GRCh37 chr1: 167,391,422-171,843,613 , GRCh38.p12 chr1: 167,422,185-171,874,473 DCAF6, SELE, 101 more genes
    nsv6299676copy number variation1nstd186human GRCh37 chr1: 168,640,538-168,666,708 , GRCh38.p12 chr1: 168,671,300-168,697,470 DPT
    nsv6296454copy number variation1nstd186human GRCh37 chr1: 168,656,133-168,662,778 , GRCh38.p12 chr1: 168,686,895-168,693,540 DPT
    nsv6245576mobile element insertion1nstd215human GRCh38 chr1: 168,712,737-168,712,737 , GRCh37.p13 chr1: 168,681,975-168,681,975 DPT
    nsv6225014insertion3nstd214human GRCh38 chr1: 168,725,218-168,725,218 , GRCh37.p13 chr1: 168,694,456-168,694,456 DPT
    nsv6220113insertion1nstd214human GRCh38 chr1: 168,725,223-168,725,223 , GRCh37.p13 chr1: 168,694,461-168,694,461 DPT
    nsv6139695copy number variation1nstd206human GRCh38 chr1: 168,686,875-168,693,560 , GRCh37.p13 chr1: 168,656,113-168,662,798 DPT
    nsv6133937copy number variation1nstd213human GRCh37 chr1: 167,800,000-169,660,001 , GRCh38.p12 chr1: 167,830,762-169,690,860 XCL2, TBX19, 38 more genes
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