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Items: 1 to 20 of 177

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5432223copy number variation1nstd206human GRCh38 chr1: 160,823,387-160,825,342 , GRCh37.p13 chr1: 160,793,177-160,795,132 LY9
    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
    nsv4784450copy number variation1nstd200human GRCh37 chr1: 160,786,779-160,789,222 , GRCh38.p12 chr1: 160,816,989-160,819,432 LY9
    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
    nsv4683645copy number variation1nstd102humanUncertain significance GRCh37 chr1: 160,786,670-161,332,308 , GRCh38.p12 chr1: 160,816,880-161,362,518 PCP4L1, NECTIN4, 32 more genes
    nsv4665274copy number variation1nstd186human GRCh37 chr1: 160,793,177-160,795,132 , GRCh38.p12 chr1: 160,823,387-160,825,342 LY9
    nsv4579770copy number variation1nstd183human GRCh37 chr1: 160,793,177-160,795,132 , GRCh38.p12 chr1: 160,823,387-160,825,342 LY9
    nsv4452657copy number variation1nstd102humanUncertain significance GRCh37 chr1: 160,744,174-162,583,871 , GRCh38.p12 chr1: 160,774,384-162,614,081 TRD-GTC2-2, KLHDC9, 104 more genes
    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
    nsv4450321copy number variation1nstd102humanUncertain significance GRCh37 chr1: 159,808,188-161,011,163 , GRCh38.p12 chr1: 159,838,398-161,041,373 LOC107985216, PPIAP37, 50 more genes
    nsv4450213copy number variation1nstd102humanUncertain significance GRCh38 chr1: 160,816,880-161,362,443 , GRCh37 chr1: 160,786,670-161,332,233 ADAMTS4, TOMM40L, 32 more genes
    nsv4346684copy number variation1nstd102humanPathogenic GRCh37 chr1: 160,369,890-175,796,325 , GRCh38.p12 chr1: 160,400,100-175,827,189 LINC00626, RN7SL861P, 359 more genes
    nsv4327204inversion1nstd166human GRCh37.p13 chr1: 156,223,026-186,411,081 , GRCh38.p12 chr1: 156,253,235-186,441,949 , FASLG, 707 more genes
    nsv4326779sequence alteration1nstd166human GRCh37.p13 chr1: 160,775,738-160,870,422 , GRCh38.p12 chr1: 160,805,948-160,900,632 LY9, CD244, 3 more genes
    nsv4070715copy number variation1nstd166human GRCh37.p13 chr1: 160,792,451-160,792,586 , GRCh38.p12 chr1: 160,822,661-160,822,796 LY9
    nsv3966913copy number variation1nstd168human GRCh38 chr1: 160,820,525-160,839,881 , GRCh37.p13 chr1: 160,790,315-160,809,671 LY9, CD244
    nsv3965619insertion1nstd168human GRCh38 chr1: 160,799,359-160,836,422 , GRCh37.p13 chr1: 160,769,149-160,806,212 LY9, CD244
    nsv3964141inversion1nstd168human GRCh38 chr1: 160,770,526-161,441,931 , GRCh37.p13 chr1: 160,740,316-161,411,721 APOA2, FCER1G, 46 more genes
    nsv3924819copy number variation1nstd102humanUncertain significance NCBI36 chr1: 158,911,295-159,168,752 , GRCh37.p13 chr1: 160,644,671-160,902,128 , GRCh38.p12 chr1: 160,674,881-160,932,338 CD48, LY9, 7 more genes
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