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Items: 1 to 20 of 157

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5898937copy number variation1nstd209human GRCh38 chr5: 139,355,392-139,359,358 , GRCh37.p13 chr5: 138,691,081-138,695,047 PAIP2
    nsv5896809copy number variation1nstd209human GRCh38 chr5: 139,359,427-139,365,265 , GRCh37.p13 chr5: 138,695,116-138,700,954 PAIP2, SLC23A1
    nsv5890701copy number variation1nstd209human GRCh38 chr5: 139,348,609-139,348,927 , GRCh37.p13 chr5: 138,684,298-138,684,616 PAIP2
    nsv5841695copy number variation1nstd209human GRCh38 chr5: 139,359,082-139,363,681 , GRCh37.p13 chr5: 138,694,771-138,699,370 PAIP2
    nsv5841444copy number variation1nstd209human GRCh38 chr5: 139,355,682-139,359,381 , GRCh37.p13 chr5: 138,691,371-138,695,070 PAIP2
    nsv5573367copy number variation1nstd207human GRCh38 chr5: 139,363,182-139,363,643 , GRCh37.p13 chr5: 138,698,871-138,699,332 PAIP2
    nsv5573216copy number variation1nstd207human GRCh38 chr5: 139,359,427-139,363,017 , GRCh37.p13 chr5: 138,695,116-138,698,706 PAIP2
    nsv5458719copy number variation1nstd206human GRCh38 chr5: 139,359,298-139,365,266 , GRCh37.p13 chr5: 138,694,987-138,700,955 PAIP2, SLC23A1
    nsv5458613copy number variation1nstd206human GRCh38 chr5: 139,339,024-139,340,488 , GRCh37.p13 chr5: 138,674,713-138,676,177 PAIP2
    nsv5381510copy number variation1nstd102humanUncertain significance GRCh37 chr5: 136,633,338-140,998,481 , GRCh38.p12 chr5: 137,297,649-141,618,914 RNA5SP195, LOC112267855, 174 more genes
    nsv5368974translocation1nstd200human GRCh38 chr11: 50,807,424-50,807,424 , GRCh38 chr5: 139,368,400-139,368,400 , GRCh37.p13 chr11: 50,766,595-50,766,595 , GRCh37.p13 chr5: 138,704,089-138,704,089 SLC23A1, PAIP2
    nsv5339338translocation1nstd200human GRCh37 chr5: 138,704,089-138,704,089 , GRCh37 chr11: 50,766,595-50,766,595 , GRCh38.p12 chr11: 50,807,424-50,807,424 , GRCh38.p12 chr5: 139,368,400-139,368,400 SLC23A1, PAIP2
    nsv5328939translocation1nstd204human GRCh37.p13 chr5: 138,695,115-138,695,115 , GRCh37.p13 chr5: 138,700,955-138,700,955 , GRCh38.p13 chr5: 139,365,266-139,365,266 , GRCh38.p13 chr5: 139,359,426-139,359,426 SLC23A1, PAIP2
    nsv5320128copy number variation1nstd204human GRCh38.p13 chr5: 139,359,416-139,363,667 , GRCh37.p13 chr5: 138,695,105-138,699,356 PAIP2
    nsv5232050copy number variation1nstd204human GRCh38.p13 chr5: 139,359,482-139,362,881 , GRCh37.p13 chr5: 138,695,171-138,698,570 PAIP2
    nsv5095596mobile element insertion1nstd203human GRCh38 chr5: 139,351,459-139,351,477 , GRCh37.p13 chr5: 138,687,148-138,687,166 PAIP2
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4945130copy number variation1nstd200human GRCh38 chr5: 138,884,159-139,363,171 , GRCh37.p13 chr5: 138,219,848-138,698,860 , SNORA74A, 11 more genes
    nsv4938865copy number variation1nstd200human GRCh38 chr5: 139,359,738-139,361,674 , GRCh37.p13 chr5: 138,695,427-138,697,363 PAIP2
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