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Items: 1 to 20 of 477

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098813copy number variation1nstd102humanPathogenic GRCh37 chr12: 176,047-34,179,852 , GRCh38.p12 chr12: 66,881-34,026,917 TDGP1, RPS4XP14, 680 more genes
    nsv7073196inversion1nstd229human GRCh38 chr12: 26,070,877-26,094,476 , GRCh37.p13 chr12: 26,223,810-26,247,409 RASSF8
    nsv7071089inversion1nstd229human GRCh38 chr12: 24,891,778-26,817,157 , GRCh37.p13 chr12: 25,044,712-26,970,090 LOC107984475, RNA5SP354, 29 more genes
    nsv7069577inversion1nstd229human GRCh38 chr12: 24,438,408-26,775,512 , GRCh37.p13 chr12: 24,591,342-26,928,445 RN7SKP262, RNU4-67P, 35 more genes
    nsv7063256inversion1nstd229human GRCh38 chr12: 25,590,859-27,919,674 , GRCh37.p13 chr12: 25,743,793-28,072,607 RARS1P1, LOC101929091, 34 more genes
    nsv7059624inversion1nstd229human GRCh38 chr12: 26,012,942-26,023,658 , GRCh37.p13 chr12: 26,165,875-26,176,591 RASSF8
    nsv6937011copy number variation1nstd229human GRCh38 chr12: 25,989,650-25,989,767 , GRCh37.p13 chr12: 26,142,583-26,142,700 RASSF8
    nsv6934268copy number variation1nstd229human GRCh38 chr12: 26,069,063-26,069,367 , GRCh37.p13 chr12: 26,221,996-26,222,300 RASSF8
    nsv6932463copy number variation1nstd229human GRCh38 chr12: 25,994,601-26,003,800 , GRCh37.p13 chr12: 26,147,534-26,156,733 RASSF8, LOC107984501
    nsv6927998copy number variation1nstd229human GRCh38 chr12: 25,993,185-25,994,162 , GRCh37.p13 chr12: 26,146,118-26,147,095 RASSF8
    nsv6925775copy number variation1nstd229human GRCh38 chr12: 26,030,926-26,037,305 , GRCh37.p13 chr12: 26,183,859-26,190,238 RASSF8
    nsv6925741copy number variation1nstd229human GRCh38 chr12: 26,076,079-26,078,084 , GRCh37.p13 chr12: 26,229,012-26,231,017 RASSF8
    nsv6925386copy number variation1nstd229human GRCh38 chr12: 26,012,542-26,016,543 , GRCh37.p13 chr12: 26,165,475-26,169,476 RASSF8
    nsv6923667copy number variation1nstd229human GRCh38 chr12: 26,005,085-26,062,388 , GRCh37.p13 chr12: 26,158,018-26,215,321 LOC107984501, RASSF8
    nsv6920568copy number variation1nstd229human GRCh38 chr12: 25,982,330-25,987,682 , GRCh37.p13 chr12: 26,135,263-26,140,615 RASSF8
    nsv6586529inversion1nstd223human GRCh38 chr12: 26,032,017-26,035,234 , GRCh37.p13 chr12: 26,184,950-26,188,167 RASSF8
    nsv6473068copy number variation1nstd223human GRCh38 chr12: 25,957,501-25,959,700 , GRCh37.p13 chr12: 26,110,434-26,112,633 RASSF8, RASSF8-AS1
    nsv6469908copy number variation1nstd223human GRCh38 chr12: 26,031,367-26,032,050 , GRCh37.p13 chr12: 26,184,300-26,184,983 RASSF8
    nsv6467981copy number variation1nstd223human GRCh38 chr12: 25,957,001-25,959,400 , GRCh37.p13 chr12: 26,109,934-26,112,333 RASSF8, RASSF8-AS1
    nsv6465991copy number variation1nstd223human GRCh38 chr12: 26,069,701-26,071,600 , GRCh37.p13 chr12: 26,222,634-26,224,533 RASSF8
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