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Items: 1 to 20 of 199

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142264insertion1nstd232human GRCh37.p13 chr3: 154,010,486-154,010,486 , GRCh38.p12 chr3: 154,292,697-154,292,697 DHX36
    nsv7047569inversion1nstd229human GRCh38 chr3: 152,490,812-161,531,961 , GRCh37.p13 chr3: 152,208,601-161,249,749 RPS2P19, LOC112268450, 128 more genes
    nsv6731379copy number variation1nstd229human GRCh38 chr3: 154,132,499-154,322,079 , GRCh37.p13 chr3: 153,850,288-154,039,868 ARHGEF26, DHX36, 1 more genes
    nsv6727067copy number variation1nstd229human GRCh38 chr3: 154,285,701-154,305,200 , GRCh37.p13 chr3: 154,003,490-154,022,989 DHX36
    nsv6725647copy number variation1nstd229human GRCh38 chr3: 154,291,334-154,294,272 , GRCh37.p13 chr3: 154,009,123-154,012,061 DHX36
    nsv6721928copy number variation1nstd229human GRCh38 chr3: 154,320,509-154,323,261 , GRCh37.p13 chr3: 154,038,298-154,041,050 DHX36
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6369141copy number variation1nstd223human GRCh38 chr3: 154,279,701-154,282,400 , GRCh37.p13 chr3: 153,997,490-154,000,189 DHX36
    nsv6364772copy number variation1nstd223human GRCh38 chr3: 154,297,572-154,298,737 , GRCh37.p13 chr3: 154,015,361-154,016,526 DHX36
    nsv6361048copy number variation1nstd223human GRCh38 chr3: 154,296,430-154,297,666 , GRCh37.p13 chr3: 154,014,219-154,015,455 DHX36
    nsv6355847copy number variation1nstd223human GRCh38 chr3: 154,306,401-154,307,600 , GRCh37.p13 chr3: 154,024,190-154,025,389 DHX36
    nsv6313678copy number variation1nstd102humanPathogenic GRCh37 chr3: 145,486,960-160,504,834 , GRCh38.p12 chr3: 145,769,173-160,787,046 RNU6-901P, RPL32P8, 229 more genes
    nsv6313632copy number variation1nstd102humanUncertain significance GRCh37 chr3: 151,147,204-154,845,718 , GRCh38.p12 chr3: 151,429,416-155,127,929 LOC105374171, ARHGEF26-AS1, 42 more genes
    nsv6290273copy number variation1nstd102humanPathogenic GRCh37 chr3: 142,729,607-157,921,084 , GRCh38.p12 chr3: 143,010,765-158,203,295 LINC02066, TM4SF1-AS1, 206 more genes
    nsv6290244copy number variation1nstd102humanPathogenic GRCh37 chr3: 143,439,359-165,252,122 , GRCh38.p12 chr3: 143,720,517-165,534,334 LOC102724145, C3orf80, 273 more genes
    nsv6259827mobile element insertion1nstd215human GRCh38 chr3: 154,312,887-154,312,887 , GRCh37.p13 chr3: 154,030,676-154,030,676 DHX36
    nsv5992089copy number variation1nstd212human GRCh38 chr3: 154,310,778-154,310,832 , GRCh37.p13 chr3: 154,028,567-154,028,621 DHX36
    nsv5957516insertion1nstd209human GRCh38 chr3: 154,310,807-154,310,807 , GRCh37.p13 chr3: 154,028,596-154,028,596 DHX36
    nsv5896853copy number variation1nstd209human GRCh38 chr3: 154,288,183-154,288,744 , GRCh37.p13 chr3: 154,005,972-154,006,533 DHX36
    nsv5692442mobile element insertion1nstd211human GRCh38 chr3: 154,312,887-154,312,887 , GRCh37.p13 chr3: 154,030,676-154,030,676 DHX36
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