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Items: 1 to 20 of 197

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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
    nsv7094047copy number variation1nstd102humanUncertain significance GRCh37 chr12: 4,368,352-9,027,607 , GRCh38.p12 chr12: 4,259,186-8,875,011 ACRBP, OR7E148P, 165 more genes
    nsv7074628inversion1nstd229human GRCh38 chr12: 5,173,229-8,663,348 , GRCh37.p13 chr12: 5,282,395-8,815,944 P3H3, LOC105369621, 141 more genes
    nsv7072221inversion1nstd229human GRCh38 chr12: 4,055,290-11,695,188 , GRCh37.p13 chr12: 4,164,456-11,848,122 RN7SL69P, KLRA1P, 285 more genes
    nsv6927492copy number variation1nstd229human GRCh38 chr12: 6,618,176-6,621,928 , GRCh37.p13 chr12: 6,727,342-6,731,094 LOC105369631, LPAR5
    nsv6925230copy number variation1nstd229human GRCh38 chr12: 6,418,401-6,902,400 , GRCh37.p13 chr12: 6,527,567-6,907,580 SPSB2, PKP2P1, 36 more genes
    nsv6920629copy number variation1nstd229human GRCh38 chr12: 6,631,201-6,635,000 , GRCh37.p13 chr12: 6,740,367-6,744,166 LPAR5
    nsv6637376copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,787-8,320,544 , GRCh38.p12 chr12: 64,621-8,167,948 GCSHP4, RNU7-1, 220 more genes
    nsv6592185inversion1nstd223human GRCh38 chr12: 6,634,045-6,634,642 , GRCh37.p13 chr12: 6,743,211-6,743,808 LPAR5
    nsv6581327inversion1nstd223human GRCh38 chr12: 6,629,913-6,630,465 , GRCh37.p13 chr12: 6,739,079-6,739,631 LPAR5
    nsv6474412copy number variation1nstd223human GRCh38 chr12: 6,627,401-6,629,200 , GRCh37.p13 chr12: 6,736,567-6,738,366 LOC105369631, LPAR5
    nsv6472373copy number variation1nstd223human GRCh38 chr12: 6,012,501-7,083,600 , GRCh37.p13 chr12: 6,121,667-7,189,876 GPR162, CD27, 71 more genes
    nsv6472196copy number variation1nstd223human GRCh38 chr12: 6,013,501-7,083,700 , GRCh37.p13 chr12: 6,122,667-7,189,876 SCARNA10, ATP5MFP5, 71 more genes
    nsv6471986copy number variation1nstd223human GRCh38 chr12: 6,625,196-6,625,565 , GRCh37.p13 chr12: 6,734,362-6,734,731 LOC105369631, LPAR5
    nsv6470472copy number variation1nstd223human GRCh38 chr12: 6,622,318-6,626,115 , GRCh37.p13 chr12: 6,731,484-6,735,281 LPAR5, LOC105369631
    nsv6470312copy number variation1nstd223human GRCh38 chr12: 6,629,501-6,633,700 , GRCh37.p13 chr12: 6,738,667-6,742,866 LPAR5
    nsv6313934copy number variation1nstd102humanUncertain significance GRCh37 chr12: 6,530,146-7,376,398 , GRCh38.p12 chr12: 6,420,980-7,223,802 VAMP1, CD27-AS1, 60 more genes
    nsv6309483copy number variation1nstd102humanUncertain significance GRCh37 chr12: 6,438,478-8,756,953 , GRCh38.p12 chr12: 6,329,312-8,604,357 ENPP7P5, GPR162, 122 more genes
    nsv6309326copy number variation2nstd102humanUncertain significance GRCh37 chr12: 6,438,478-8,248,686 , GRCh38.p12 chr12: 6,329,312-8,096,090 NANOGNB, SCNN1A, 94 more genes
    nsv6304064copy number variation1nstd186human GRCh37 chr12: 6,736,526-6,738,269 , GRCh38.p12 chr12: 6,627,360-6,629,103 LPAR5, LOC105369631
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