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Items: 1 to 20 of 192

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137099copy number variation1nstd102humanPathogenic GRCh37 chr12: 11,463,270-14,019,142 , GRCh38.p12 chr12: 11,310,336-13,866,208 HTR7P1, RPL37AP9, 55 more genes
    nsv7098813copy number variation1nstd102humanPathogenic GRCh37 chr12: 176,047-34,179,852 , GRCh38.p12 chr12: 66,881-34,026,917 TDGP1, RPS4XP14, 680 more genes
    nsv7064011inversion1nstd229human GRCh38 chr12: 11,255,910-17,864,916 , GRCh37.p13 chr12: 11,408,826-18,017,850 MGP, MIR3974, 108 more genes
    nsv6937655copy number variation1nstd229human GRCh38 chr12: 12,936,545-12,949,548 , GRCh37.p13 chr12: 13,089,479-13,102,482 GPRC5D, GPRC5D-AS1
    nsv6933366copy number variation1nstd229human GRCh38 chr12: 12,947,865-12,957,642 , GRCh37.p13 chr12: 13,100,799-13,110,576 GPRC5D, GPRC5D-AS1
    nsv6932098copy number variation1nstd229human GRCh38 chr12: 12,943,663-12,943,695 , GRCh37.p13 chr12: 13,096,597-13,096,629 GPRC5D, GPRC5D-AS1
    nsv6920204copy number variation1nstd229human GRCh38 chr12: 12,951,408-12,961,428 , GRCh37.p13 chr12: 13,104,342-13,114,362 GPRC5D-AS1, GPRC5D
    nsv6634456copy number variation1nstd102humanPathogenic GRCh37 chr12: 10,853,887-24,103,810 , GRCh38.p12 chr12: 10,701,288-23,950,876 TAS2R15P, LOC105369673, 209 more genes
    nsv6470183copy number variation1nstd223human GRCh38 chr12: 12,756,563-12,941,912 , GRCh37.p13 chr12: 12,909,497-13,094,846 STX8P1, RPL13AP20, 9 more genes
    nsv6309465copy number variation2nstd102humanUncertain significance GRCh37 chr12: 11,803,062-15,835,885 , GRCh38.p12 chr12: 11,650,128-15,682,951 LRP6, APOLD1, 78 more genes
    nsv6303053copy number variation1nstd186human GRCh37 chr12: 13,108,871-13,109,452 , GRCh38.p12 chr12: 12,955,937-12,956,518 GPRC5D, GPRC5D-AS1
    nsv6132720copy number variation1nstd213human GRCh37 chr12: 9,040,000-17,930,001 , GRCh38.p12 chr12: 8,887,404-17,777,067 A2M, A2MP1, 215 more genes
    nsv6132422copy number variation1nstd213human GRCh37 chr12: 190,000-30,830,001 , GRCh38.p12 chr12: 80,834-30,677,067 , A2M, 622 more genes
    nsv6132325copy number variation1nstd213human GRCh37 chr12: 13,090,000-13,460,001 , GRCh38.p12 chr12: 12,937,066-13,307,067 EMP1, HEBP1, 7 more genes
    nsv6132215copy number variation1nstd213human GRCh37 chr12: 11,360,000-16,150,001 , GRCh38.p12 chr12: 11,207,094-15,997,067 ARHGDIB, ART4, 93 more genes
    nsv6132146copy number variation1nstd213human GRCh37 chr12: 12,970,000-13,590,001 , GRCh38.p12 chr12: 12,817,066-13,437,067 EMP1, GPRC5A, 14 more genes
    nsv6132138copy number variation1nstd213human GRCh37 chr12: 11,250,000-19,950,001 , GRCh38.p12 chr12: 11,097,401-19,797,067 ARHGDIB, ART4, 139 more genes
    nsv5977383insertion1nstd209human GRCh38 chr12: 12,944,795-12,944,795 , GRCh37.p13 chr12: 13,097,729-13,097,729 GPRC5D, GPRC5D-AS1
    nsv5728260mobile element insertion1nstd211human GRCh38 chr12: 12,938,963-12,938,963 , GRCh37.p13 chr12: 13,091,897-13,091,897 GPRC5D-AS1, GPRC5D
    nsv5700055mobile element insertion1nstd211human GRCh38 chr12: 12,944,850-12,944,850 , GRCh37.p13 chr12: 13,097,784-13,097,784 GPRC5D, GPRC5D-AS1
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