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Items: 1 to 20 of 130

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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
    nsv6935645copy number variation1nstd229human GRCh38 chr12: 31,318,301-31,323,300 , GRCh37.p13 chr12: 31,471,235-31,476,234 FLJ13224, SINHCAF
    nsv6935238copy number variation1nstd229human GRCh38 chr12: 31,323,901-31,369,000 , GRCh37.p13 chr12: 31,476,835-31,521,934 LINC02387, SINHCAF, 1 more genes
    nsv6933269copy number variation1nstd229human GRCh38 chr12: 31,007,302-31,395,281 , GRCh37.p13 chr12: 31,160,237-31,548,215 RNU6-618P, MTND6P26, 15 more genes
    nsv6471652copy number variation1nstd223human GRCh38 chr12: 31,323,801-31,326,400 , GRCh37.p13 chr12: 31,476,735-31,479,334 SINHCAF, FLJ13224
    nsv6132241copy number variation1nstd213human GRCh37 chr12: 31,410,000-34,000,001 , GRCh38.p12 chr12: 31,257,066-33,847,066 ASS1P14, BICD1, 39 more genes
    nsv6132240copy number variation1nstd213human GRCh37 chr12: 30,730,000-31,780,001 , GRCh38.p12 chr12: 30,577,066-31,627,067 CAPRIN2, DENND5B, 28 more genes
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4704595copy number variation1nstd195human GRCh37 chr12: 31,345,251-31,703,051 , GRCh38.p12 chr12: 31,192,317-31,550,117 MRPL30P2, LINC02387, 13 more genes
    nsv4679887copy number variation1nstd189human GRCh37.p13 chr12: 31,245,904-31,613,301 , GRCh38.p12 chr12: 31,092,970-31,460,367 , GRCh38.p12 chr12|NT_187587.1: 1-238,139 DDX11, SINHCAF, 13 more genes
    nsv4678888copy number variation1nstd189human GRCh37.p13 chr12: 31,216,608-31,504,002 , GRCh38.p12 chr12: 31,063,674-31,351,068 , GRCh38.p12 chr12|NT_187587.1: 1-238,139 DDX11, SINHCAF, 11 more genes
    nsv4674941copy number variation1nstd102humanPathogenic GRCh37 chr12: 274,676-37,869,301 , GRCh38.p12 chr12: 165,510-37,475,499 LOC105376675, ATF7IP, 682 more genes
    nsv4455797copy number variation1nstd102humanUncertain significance GRCh37 chr12: 31,453,473-33,040,145 , GRCh38.p12 chr12: 31,300,539-32,887,211 RPL12P32, LOC100132543, 33 more genes
    nsv4455458copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-34,496,628 , GRCh38.p12 chr12: 64,620-34,343,693 EMP1, PLBD1-AS1, 684 more genes
    nsv4324772inversion1nstd166human GRCh37.p13 chr12: 27,368,635-91,765,744 , GRCh38.p12 chr12: 27,215,702-91,371,967 , ATP2B1, 1101 more genes
    nsv3924262copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-34,835,837 , GRCh38 chr12: 64,620-34,682,902 , NCBI36 chr12: 44,047-34,727,104 ENO2, SLC6A13, 684 more genes
    nsv3920847inversion1nstd102humanUncertain significance GRCh38.p12 chr12: 26,217,318-53,967,754 , GRCh37 chr12: 26,370,251-54,361,538 , ASIC1, 491 more genes
    nsv3917488copy number variation1nstd102humanPathogenic NCBI36 chr12: 192,403-33,971,115 , GRCh37 chr12: 322,142-34,079,848 , GRCh38 chr12: 212,976-33,926,913 LOC374443, LINC00937, 674 more genes
    nsv3916538copy number variation1nstd102humanPathogenic GRCh38 chr12: 77,187-34,380,176 , GRCh37 chr12: 282,465-34,533,111 , NCBI36 chr12: 56,614-34,424,378 A2M, DSTNP2, 684 more genes
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