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Items: 1 to 20 of 698

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131236insertion1nstd186human GRCh37 chr14: 92,125,068-92,125,104 , GRCh38.p12 chr14: 91,658,724-91,658,760 , GRCh38.p12 chr14|NT_187598.1: 126,519-126,555 CATSPERB
    nsv6131106insertion1nstd186human GRCh37 chr14: 92,247,261-92,247,302 , GRCh38.p12 chr14: 91,780,917-91,780,958 , GRCh38.p12 chr14|NT_187598.1: 248,712-248,753 TC2N
    nsv6130455insertion1nstd186human GRCh37 chr14: 92,101,080-92,101,080 , GRCh38.p12 chr14|NT_187598.1: 98,870-98,870 , GRCh38.p12 chr14: 91,634,736-91,634,736 CATSPERB
    nsv6121643copy number variation1nstd186human GRCh37 chr14: 92,023,420-92,023,729 , GRCh38.p12 chr14|NT_187598.1: 21,212-21,521 , GRCh38.p12 chr14: 91,557,076-91,557,385 LOC101928957
    nsv4849489copy number variation1nstd200human GRCh37 chr14: 92,220,055-92,227,656 , GRCh38.p12 chr14|NT_187598.1: 221,506-229,107 , GRCh38.p12 chr14: 91,753,711-91,761,312 0
    nsv4849488copy number variation1nstd200human GRCh37 chr14: 92,183,921-92,184,136 , GRCh38.p12 chr14|NT_187598.1: 185,372-185,587 , GRCh38.p12 chr14: 91,717,577-91,717,792 CATSPERB
    nsv4849487copy number variation1nstd200human GRCh37 chr14: 92,094,108-92,094,220 , GRCh38.p12 chr14: 91,627,764-91,627,876 , GRCh38.p12 chr14|NT_187598.1: 91,896-92,008 CATSPERB
    nsv4849486copy number variation1nstd200human GRCh37 chr14: 92,051,483-92,051,603 , GRCh38.p12 chr14|NT_187598.1: 49,275-49,395 , GRCh38.p12 chr14: 91,585,139-91,585,259 CATSPERB
    nsv4759685insertion1nstd199human GRCh37 chr14: 92,302,919-92,302,919 , GRCh38.p12 chr14|NT_187598.1: 304,370-304,370 , GRCh38.p12 chr14: 91,836,575-91,836,575 TC2N
    nsv4759650insertion1nstd199human GRCh37 chr14: 92,125,056-92,125,056 , GRCh38.p12 chr14: 91,658,712-91,658,712 , GRCh38.p12 chr14|NT_187598.1: 126,507-126,507 CATSPERB
    nsv4759386insertion1nstd199human GRCh37 chr14: 92,116,012-92,116,012 , GRCh38.p12 chr14|NT_187598.1: 117,463-117,463 , GRCh38.p12 chr14: 91,649,668-91,649,668 CATSPERB
    nsv4752519insertion1nstd199human GRCh37 chr14: 92,101,077-92,101,077 , GRCh38.p12 chr14|NT_187598.1: 98,867-98,867 , GRCh38.p12 chr14: 91,634,733-91,634,733 CATSPERB
    nsv4735829copy number variation1nstd199human GRCh37 chr14: 92,023,507-92,023,686 , GRCh38.p12 chr14|NT_187598.1: 21,299-21,478 , GRCh38.p12 chr14: 91,557,163-91,557,342 LOC101928957
    nsv4724775insertion2nstd186human GRCh37 chr14: 92,116,005-92,116,005 , GRCh38.p12 chr14: 91,649,661-91,649,661 , GRCh38.p12 chr14|NT_187598.1: 117,456-117,456 CATSPERB
    nsv4724042insertion1nstd186human GRCh37 chr14: 92,247,249-92,247,249 , GRCh38.p12 chr14: 91,780,905-91,780,905 , GRCh38.p12 chr14|NT_187598.1: 248,700-248,700 TC2N
    nsv4716987mobile element insertion1nstd186human GRCh37 chr14: 92,125,053-92,125,053 , GRCh38.p12 chr14: 91,658,709-91,658,709 , GRCh38.p12 chr14|NT_187598.1: 126,504-126,504 CATSPERB
    nsv4691082mobile element insertion1nstd186human GRCh37 chr14: 92,247,261-92,247,261 , GRCh38.p12 chr14|NT_187598.1: 248,712-248,712 , GRCh38.p12 chr14: 91,780,917-91,780,917 TC2N
    nsv4687429mobile element insertion1nstd186human GRCh37 chr14: 92,116,020-92,116,020 , GRCh38.p12 chr14: 91,649,676-91,649,676 , GRCh38.p12 chr14|NT_187598.1: 117,471-117,471 CATSPERB
    nsv4687010mobile element insertion1nstd186human GRCh37 chr14: 92,125,068-92,125,068 , GRCh38.p12 chr14: 91,658,724-91,658,724 , GRCh38.p12 chr14|NT_187598.1: 126,519-126,519 CATSPERB
    nsv4578135mobile element insertion1nstd166human GRCh37.p13 chr14: 92,043,766-92,043,766 , GRCh38.p12 chr14|NT_187598.1: 41,558-41,558 , GRCh38.p12 chr14: 91,577,422-91,577,422 LOC101928957
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