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Items: 1 to 20 of 148

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5557355sequence alteration1nstd206human GRCh38 chr12: 127,331,393-127,331,949 , GRCh37.p13 chr12: 127,815,938-127,816,494 LINC02375
    nsv5497473copy number variation1nstd206human GRCh38 chr12: 126,251,831-127,523,787 , GRCh37.p13 chr12: 126,736,377-128,008,332 RNU1-104P, LOC121296, 28 more genes
    nsv5274516copy number variation1nstd204human GRCh38.p13 chr12: 127,125,401-127,568,500 , GRCh37.p13 chr12: 127,609,946-128,053,045 LOC107984450, LOC105370066, 8 more genes
    nsv4993853copy number variation1nstd200human GRCh38 chr12: 126,501,426-128,016,593 , GRCh37.p13 chr12: 126,985,972-128,501,138 LINC02376, LINC02393, 29 more genes
    nsv4679787copy number variation1nstd189human GRCh37.p13 chr12: 127,585,367-128,052,533 , GRCh38.p12 chr12: 127,100,822-127,567,988 LOC100420116, LINC02375, 8 more genes
    nsv4672592copy number variation1nstd186human GRCh37 chr12: 127,430,503-127,812,976 , GRCh38.p12 chr12: 126,945,957-127,328,431 RNU1-104P, LOC105370062, 8 more genes
    nsv4672220copy number variation1nstd186human GRCh37 chr12: 127,817,403-128,009,847 , GRCh38.p12 chr12: 127,332,858-127,525,302 LINC02375, LOC105370066, 1 more genes
    nsv4658527copy number variation1nstd186human GRCh37 chr12: 127,817,403-128,009,847 , GRCh38.p12 chr12: 127,332,858-127,525,302 LINC02375, LOC105370066, 1 more genes
    nsv4609768copy number variation1nstd183human GRCh37 chr12: 127,738,164-127,851,874 , GRCh38.p12 chr12: 127,253,619-127,367,329 LOC100420116, RNU1-104P, 2 more genes
    nsv4606882copy number variation1nstd183human GRCh37 chr12: 127,810,511-127,811,140 , GRCh38.p12 chr12: 127,325,966-127,326,595 LINC02375
    nsv4547884insertion1nstd166human GRCh37.p13 chr12: 127,817,563-127,817,563 , GRCh38.p12 chr12: 127,333,018-127,333,018 LINC02375
    nsv4456888copy number variation1nstd102humanUncertain significance GRCh37 chr12: 126,470,636-133,777,902 , GRCh38.p12 chr12: 125,986,090-133,201,316 LINC02347, LOC107987176, 145 more genes
    nsv4455865copy number variation1nstd102humanUncertain significance GRCh37 chr12: 126,987,740-128,503,756 , GRCh38.p12 chr12: 126,503,194-128,019,211 LOC107984449, LOC100419932, 29 more genes
    nsv4455692copy number variation1nstd102humanPathogenic GRCh37 chr12: 122,169,403-129,084,163 , GRCh38.p12 chr12: 121,731,497-128,599,618 LOC107987176, LRRC43, 147 more genes
    nsv4430939copy number variation1nstd174human GRCh37 chr12: 127,276,861-127,812,976 , GRCh38.p12 chr12: 126,792,315-127,328,431 LOC105370061, LINC02375, 12 more genes
    nsv4349911copy number variation1nstd102humanPathogenic GRCh37 chr12: 125,451,405-133,810,935 , GRCh38.p12 chr12: 124,966,859-133,234,349 LOC107987177, GOLGA3, 159 more genes
    nsv4230041copy number variation1nstd166human GRCh37.p13 chr12: 127,811,289-127,811,888 , GRCh38.p12 chr12: 127,326,744-127,327,343 LINC02375
    nsv4216340copy number variation1nstd166human GRCh37.p13 chr12: 126,752,298-127,889,686 , GRCh38.p12 chr12: 126,267,752-127,405,141 LOC107984448, RNU1-104P, 26 more genes
    nsv3924220copy number variation1nstd102humanPathogenic GRCh38 chr12: 115,131,583-133,166,920 , NCBI36 chr12: 114,053,771-132,253,579 , GRCh37 chr12: 115,569,388-133,743,506 LOC105370080, LINC02985, 376 more genes
    nsv3923612copy number variation1nstd102humanPathogenic GRCh38 chr12: 120,718,786-127,500,215 , GRCh37 chr12: 121,156,589-127,984,760 , NCBI36 chr12: 119,640,972-126,550,713 NCOR2, LOC105378258, 161 more genes
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