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Items: 1 to 20 of 1693

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6118394copy number variation1nstd186human GRCh37 chr3: 25,291,341-25,291,415 , GRCh38.p12 chr3: 25,249,850-25,249,924 , RARB
    nsv5966664insertion1nstd209human GRCh38 chr3: 24,946,366-24,946,366 , GRCh37.p13 chr3: 24,987,857-24,987,857 RARB
    nsv5965931insertion1nstd209human GRCh38 chr3: 25,007,604-25,007,604 , GRCh37.p13 chr3: 25,049,095-25,049,095 RARB
    nsv5961356insertion1nstd209human GRCh38 chr3: 25,081,607-25,081,607 , GRCh37.p13 chr3: 25,123,098-25,123,098 RARB
    nsv5960454insertion1nstd209human GRCh38 chr3: 25,069,212-25,069,212 , GRCh37.p13 chr3: 25,110,703-25,110,703 RARB
    nsv5960271insertion1nstd209human GRCh38 chr3: 25,348,404-25,348,404 , GRCh37.p13 chr3: 25,389,895-25,389,895 RARB
    nsv5954804insertion1nstd209human GRCh38 chr3: 25,236,956-25,236,956 , GRCh37.p13 chr3: 25,278,447-25,278,447 , RARB
    nsv5952026insertion1nstd209human GRCh38 chr3: 24,877,346-24,877,346 , GRCh37.p13 chr3: 24,918,837-24,918,837 RARB
    nsv5948740insertion1nstd209human GRCh38 chr3: 24,912,975-24,912,975 , GRCh37.p13 chr3: 24,954,466-24,954,466 RARB
    nsv5948275insertion1nstd209human GRCh38 chr3: 24,972,314-24,972,314 , GRCh37.p13 chr3: 25,013,805-25,013,805 RARB
    nsv5948091insertion1nstd209human GRCh38 chr3: 25,130,900-25,130,900 , GRCh37.p13 chr3: 25,172,391-25,172,391 RARB
    nsv5906357copy number variation1nstd209human GRCh38 chr3: 24,918,480-25,031,821 , GRCh37.p13 chr3: 24,959,971-25,073,312 RARB, RNA5SP125, 1 more genes
    nsv5902498copy number variation1nstd209human GRCh38 chr3: 25,195,103-25,237,559 , GRCh37.p13 chr3: 25,236,594-25,279,050 , RARB
    nsv5900382copy number variation1nstd209human GRCh38 chr3: 25,192,775-25,193,241 , GRCh37.p13 chr3: 25,234,266-25,234,732 RARB
    nsv5899180copy number variation1nstd209human GRCh38 chr3: 24,883,668-24,884,001 , GRCh37.p13 chr3: 24,925,159-24,925,492 RARB
    nsv5899065copy number variation1nstd209human GRCh38 chr3: 25,249,850-25,249,921 , GRCh37.p13 chr3: 25,291,341-25,291,412 , RARB
    nsv5897431copy number variation1nstd209human GRCh38 chr3: 25,508,187-25,510,290 , GRCh37.p13 chr3: 25,549,678-25,551,781 RARB
    nsv5896840copy number variation1nstd209human GRCh38 chr3: 25,169,003-25,183,208 , GRCh37.p13 chr3: 25,210,494-25,224,699 RARB
    nsv5895784copy number variation1nstd209human GRCh38 chr3: 24,989,396-24,990,757 , GRCh37.p13 chr3: 25,030,887-25,032,248 RARB
    nsv5893777copy number variation1nstd209human GRCh38 chr3: 25,341,456-25,342,036 , GRCh37.p13 chr3: 25,382,947-25,383,527 RARB
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