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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
    nsv7098788copy number variation1nstd102humanUncertain significance GRCh37 chr4: 101,947,022-107,268,849 , GRCh38.p12 chr4: 101,025,865-106,347,692 LOC107986297, LOC100288914, 60 more genes
    nsv7048086inversion1nstd229human GRCh38 chr4: 100,058,481-107,564,371 , GRCh37.p13 chr4: 100,979,638-108,485,528 ACTR6P1, INTS12, 79 more genes
    nsv7044544inversion1nstd229human GRCh38 chr4: 98,964,941-108,185,877 , GRCh37.p13 chr4: 99,886,092-109,107,033 LOC102725220, TACR3, 117 more genes
    nsv6757580copy number variation1nstd229human GRCh38 chr4: 105,484,900-105,643,367 , GRCh37.p13 chr4: 106,406,057-106,564,524 ARHGEF38, EEF1A1P9, 4 more genes
    nsv6756305copy number variation1nstd229human GRCh38 chr4: 105,561,966-105,563,739 , GRCh37.p13 chr4: 106,483,123-106,484,896 ARHGEF38, ARHGEF38-IT1
    nsv6751386copy number variation1nstd229human GRCh38 chr4: 105,539,601-105,581,049 , GRCh37.p13 chr4: 106,460,758-106,502,206 ARHGEF38, LOC105377352, 1 more genes
    nsv6749849copy number variation1nstd229human GRCh38 chr4: 103,966,147-109,668,724 , GRCh37.p13 chr4: 104,887,304-110,589,880 CYP2U1-AS1, OSTC, 66 more genes
    nsv6747411copy number variation1nstd229human GRCh38 chr4: 105,556,101-105,565,800 , GRCh37.p13 chr4: 106,477,258-106,486,957 ARHGEF38, ARHGEF38-IT1
    nsv6746800copy number variation1nstd229human GRCh38 chr4: 104,857,254-105,989,113 , GRCh37.p13 chr4: 105,778,411-106,910,270 PIMREGP2, ARHGEF38-IT1, 18 more genes
    nsv6744327copy number variation1nstd229human GRCh38 chr4: 105,561,085-105,561,495 , GRCh37.p13 chr4: 106,482,242-106,482,652 ARHGEF38, ARHGEF38-IT1
    nsv6738579copy number variation1nstd229human GRCh38 chr4: 105,570,420-105,581,445 , GRCh37.p13 chr4: 106,491,577-106,502,602 ARHGEF38, ARHGEF38-IT1
    nsv6391952copy number variation1nstd223human GRCh38 chr4: 105,554,484-105,666,351 , GRCh37.p13 chr4: 106,475,641-106,587,508 ARHGEF38, ARHGEF38-IT1
    nsv6378864copy number variation1nstd223human GRCh38 chr4: 105,539,601-105,581,046 , GRCh37.p13 chr4: 106,460,758-106,502,203 ARHGEF38, ARHGEF38-IT1, 1 more genes
    nsv6313878copy number variation1nstd102humanPathogenic GRCh37 chr4: 104,715,235-145,252,595 , GRCh38.p12 chr4: 103,794,078-144,331,443 LINC00613, GYPA, 448 more genes
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 more genes
    nsv6291428copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 95,490,755-109,977,216 , GRCh38.p12 chr4: 94,569,604-109,056,060 ADH1A, ADH1B, 157 more genes
    nsv6280884insertion1nstd214human GRCh38 chr4: 105,561,504-105,561,504 , GRCh37.p13 chr4: 106,482,661-106,482,661 ARHGEF38, ARHGEF38-IT1
    nsv6263760copy number variation1nstd214human GRCh38 chr4: 105,561,396-105,561,448 , GRCh37.p13 chr4: 106,482,553-106,482,605 ARHGEF38, ARHGEF38-IT1
    nsv6165988copy number variation1nstd214human GRCh38 chr4: 105,561,424-105,561,478 , GRCh37.p13 chr4: 106,482,581-106,482,635 ARHGEF38, ARHGEF38-IT1
    nsv6163649copy number variation1nstd214human GRCh38 chr4: 105,561,398-105,561,457 , GRCh37.p13 chr4: 106,482,555-106,482,614 ARHGEF38-IT1, ARHGEF38
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