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Items: 1 to 20 of 189

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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
    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
    nsv6930387copy number variation1nstd229human GRCh38 chr12: 26,199,657-26,211,442 , GRCh37.p13 chr12: 26,352,590-26,364,375 ITPR2-AS1, SSPN
    nsv6921984copy number variation1nstd229human GRCh38 chr12: 26,167,655-26,225,967 , GRCh37.p13 chr12: 26,320,588-26,378,900 SSPN, ITPR2-AS1
    nsv6470964copy number variation1nstd223human GRCh38 chr12: 26,208,401-26,209,500 , GRCh37.p13 chr12: 26,361,334-26,362,433 ITPR2-AS1, SSPN
    nsv6314083copy number variation1nstd102humanPathogenic GRCh37 chr12: 17,884,992-26,704,895 , GRCh38.p12 chr12: 17,732,058-26,551,962 SLCO1B1, RERGL, 105 more genes
    nsv6290811copy number variation1nstd102humanPathogenic GRCh37 chr12: 23,693,737-29,545,102 , GRCh38.p12 chr12: 23,540,803-29,392,169 LOC105369709, REP15, 74 more genes
    nsv6132687copy number variation1nstd213human GRCh37 chr12: 26,090,000-26,790,001 , GRCh38.p12 chr12: 25,937,067-26,637,068 ITPR2, SSPN, 9 more genes
    nsv6132683copy number variation1nstd213human GRCh37 chr12: 23,270,000-28,660,001 , GRCh38.p12 chr12: 23,117,066-28,507,068 , IRAG2, 68 more genes
    nsv6132422copy number variation1nstd213human GRCh37 chr12: 190,000-30,830,001 , GRCh38.p12 chr12: 80,834-30,677,067 , A2M, 622 more genes
    nsv6132235copy number variation1nstd213human GRCh37 chr12: 26,030,000-27,870,001 , GRCh38.p12 chr12: 25,877,067-27,717,068 ITPR2, RASSF8, 26 more genes
    nsv6132234copy number variation1nstd213human GRCh37 chr12: 25,870,000-26,830,001 , GRCh38.p12 chr12: 25,717,066-26,677,068 RASSF8, BHLHE41, 12 more genes
    nsv5923742copy number variation1nstd209human GRCh38 chr12: 21,398,810-28,763,815 , GRCh37.p13 chr12: 21,551,744-28,916,748 , LOC105369710, 101 more genes
    nsv5916901copy number variation1nstd209human GRCh38 chr12: 21,398,719-28,763,765 , GRCh37.p13 chr12: 21,551,653-28,916,698 , LOC105369704, 101 more genes
    nsv5912980copy number variation1nstd209human GRCh38 chr12: 25,481,034-28,003,055 , GRCh37.p13 chr12: 25,633,968-28,155,988 , ITPR2-AS1, 36 more genes
    nsv5727953mobile element insertion1nstd211human GRCh38 chr12: 26,215,698-26,215,698 , GRCh37.p13 chr12: 26,368,631-26,368,631 ITPR2-AS1, SSPN
    nsv5715033mobile element insertion1nstd211human GRCh38 chr12: 26,214,893-26,214,893 , GRCh37.p13 chr12: 26,367,826-26,367,826 ITPR2-AS1, SSPN
    nsv5500265copy number variation1nstd206human GRCh38 chr12: 26,214,137-26,214,237 , GRCh37.p13 chr12: 26,367,070-26,367,170 SSPN, ITPR2-AS1
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