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Items: 1 to 20 of 131

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6129909mobile element insertion1nstd186human GRCh37 chr12: 128,777,557-128,777,608 , GRCh38.p12 chr12: 128,293,012-128,293,063 TMEM132C, MIR3612
    nsv5979266insertion1nstd209human GRCh38 chr12: 128,292,999-128,292,999 , GRCh37.p13 chr12: 128,777,544-128,777,544 TMEM132C, MIR3612
    nsv5931772copy number variation1nstd209human GRCh38 chr12: 128,292,657-128,292,715 , GRCh37.p13 chr12: 128,777,202-128,777,260 MIR3612, TMEM132C
    nsv5848700copy number variation2nstd209human GRCh38 chr12: 128,294,016-128,295,156 , GRCh37.p13 chr12: 128,778,561-128,779,701 TMEM132C, MIR3612
    nsv5718754mobile element insertion2nstd211human GRCh38 chr12: 128,293,012-128,293,012 , GRCh37.p13 chr12: 128,777,557-128,777,557 MIR3612, TMEM132C
    nsv5597488copy number variation1nstd207human GRCh38 chr12: 128,292,646-128,292,704 , GRCh37.p13 chr12: 128,777,191-128,777,249 MIR3612, TMEM132C
    nsv5560673mobile element insertion1nstd206human GRCh38 chr12: 128,293,012-128,293,063 , GRCh37.p13 chr12: 128,777,557-128,777,608 MIR3612, TMEM132C
    nsv5196510mobile element insertion1nstd203human GRCh38 chr12: 128,293,006-128,293,012 , GRCh37.p13 chr12: 128,777,551-128,777,557 TMEM132C, MIR3612
    nsv5185664mobile element insertion1nstd203human GRCh38 chr12: 128,293,003-128,293,012 , GRCh37.p13 chr12: 128,777,548-128,777,557 TMEM132C, MIR3612
    nsv5180540mobile element insertion1nstd203human GRCh38 chr12: 128,292,999-128,293,012 , GRCh37.p13 chr12: 128,777,544-128,777,557 TMEM132C, MIR3612
    nsv4993861copy number variation1nstd200human GRCh38 chr12: 128,258,840-128,629,947 , GRCh37.p13 chr12: 128,743,385-129,114,492 MIR3612, TMEM132C, 1 more genes
    nsv4833320copy number variation1nstd200human GRCh37 chr12: 128,743,385-129,114,492 , GRCh38.p12 chr12: 128,258,840-128,629,947 TMEM132C, MIR3612, 1 more genes
    nsv4734640copy number variation1nstd199human GRCh37 chr12: 128,777,195-128,777,253 , GRCh38.p12 chr12: 128,292,650-128,292,708 MIR3612, TMEM132C
    nsv4723372mobile element insertion1nstd186human GRCh37 chr12: 128,777,544-128,777,544 , GRCh38.p12 chr12: 128,292,999-128,292,999 TMEM132C, MIR3612
    nsv4606539copy number variation1nstd183human GRCh37 chr12: 128,443,579-128,861,474 , GRCh38.p12 chr12: 127,959,034-128,376,929 TMEM132C, MIR3612, 6 more genes
    nsv4567694mobile element insertion1nstd166human GRCh37.p13 chr12: 128,777,544-128,777,544 , GRCh38.p12 chr12: 128,292,999-128,292,999 MIR3612, TMEM132C
    nsv4512433mobile element insertion1nstd166human GRCh37.p13 chr12: 128,778,386-128,778,386 , GRCh38.p12 chr12: 128,293,841-128,293,841 TMEM132C, MIR3612
    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
    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
    nsv4455426copy number variation1nstd102humanUncertain significance GRCh37 chr12: 128,503,810-130,456,374 , GRCh38.p12 chr12: 128,019,265-129,971,829 LINC02369, LOC105370074, 17 more genes
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