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Items: 1 to 20 of 315

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146892copy number variation1nstd232human GRCh37.p13 chr12: 6,602,136-6,602,220 , GRCh38.p12 chr12: 6,492,970-6,493,054 NCAPD2, MRPL51
    nsv7145699copy number variation1nstd232human GRCh37.p13 chr12: 6,635,535-6,635,610 , GRCh38.p12 chr12: 6,526,369-6,526,444 NCAPD2
    nsv7144221copy number variation1nstd232human GRCh37.p13 chr12: 6,639,982-6,640,084 , GRCh38.p12 chr12: 6,530,816-6,530,918 NCAPD2, GAPDH-DT
    nsv7143138copy number variation1nstd232human GRCh37.p13 chr12: 6,623,558-6,623,628 , GRCh38.p12 chr12: 6,514,392-6,514,462 NCAPD2
    nsv7141114copy number variation1nstd232human GRCh37.p13 chr12: 6,613,336-6,613,397 , GRCh38.p12 chr12: 6,504,170-6,504,231 NCAPD2
    nsv7140290insertion1nstd232human GRCh37.p13 chr12: 6,627,126-6,627,126 , GRCh38.p12 chr12: 6,517,960-6,517,960 NCAPD2
    nsv7139441copy number variation1nstd232human GRCh37.p13 chr12: 6,626,663-6,626,758 , GRCh38.p12 chr12: 6,517,497-6,517,592 NCAPD2
    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
    nsv6935141copy number variation1nstd229human GRCh38 chr12: 6,528,504-6,528,837 , GRCh37.p13 chr12: 6,637,670-6,638,003 NCAPD2, GAPDH-DT
    nsv6929302copy number variation1nstd229human GRCh38 chr12: 6,526,501-6,534,300 , GRCh37.p13 chr12: 6,635,667-6,643,466 GAPDH, NCAPD2, 1 more genes
    nsv6926653copy number variation1nstd229human GRCh38 chr12: 6,512,247-6,515,863 , GRCh37.p13 chr12: 6,621,413-6,625,029 NCAPD2
    nsv6926594copy number variation1nstd229human GRCh38 chr12: 6,520,389-6,520,455 , GRCh37.p13 chr12: 6,629,555-6,629,621 NCAPD2
    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
    nsv6922286copy number variation1nstd229human GRCh38 chr12: 6,158,793-6,527,112 , GRCh37.p13 chr12: 6,267,959-6,636,278 SCARNA10, PKP2P1, 21 more genes
    nsv6637376copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,787-8,320,544 , GRCh38.p12 chr12: 64,621-8,167,948 GCSHP4, RNU7-1, 220 more genes
    nsv6621832copy number variation1nstd224human GRCh37 chr12: 6,457,963-6,676,977 , GRCh38.p12 chr12: 6,348,797-6,567,811 LTBR, NOP2, 16 more genes
    nsv6591715inversion1nstd223human GRCh38 chr12: 6,505,734-6,505,939 , GRCh37.p13 chr12: 6,614,900-6,615,105 NCAPD2
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