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Items: 1 to 20 of 356

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4804906copy number variation1nstd200human GRCh37 chr3: 153,966,091-153,984,817 , GRCh38.p12 chr3|NT_187533.1: 15,015-33,741 , GRCh38.p12 chr3: 154,248,302-154,267,028 , ARHGEF26, 1 more genes
    nsv4798078copy number variation1nstd200human GRCh37 chr3: 153,948,127-153,950,740 , GRCh38.p12 chr3|NT_187533.1: 49,092-51,705 , GRCh38.p12 chr3: 154,230,338-154,232,951 ARHGEF26
    nsv4798077copy number variation1nstd200human GRCh37 chr3: 153,917,653-153,917,717 , GRCh38.p12 chr3: 154,199,864-154,199,928 , GRCh38.p12 chr3|NT_187533.1: 82,115-82,179 ARHGEF26
    nsv4798076copy number variation1nstd200human GRCh37 chr3: 153,885,519-153,885,649 , GRCh38.p12 chr3: 154,167,730-154,167,860 , GRCh38.p12 chr3|NT_187533.1: 117,356-117,486 ARHGEF26
    nsv4769147insertion1nstd186human GRCh37 chr3: 153,898,407-153,898,407 , GRCh38.p12 chr3|NT_187533.1: 104,604-104,604 , GRCh38.p12 chr3: 154,180,618-154,180,618 ARHGEF26
    nsv4757839insertion1nstd199human GRCh37 chr3: 153,898,407-153,898,407 , GRCh38.p12 chr3|NT_187533.1: 104,604-104,604 , GRCh38.p12 chr3: 154,180,618-154,180,618 ARHGEF26
    nsv4743498copy number variation1nstd199human GRCh37 chr3: 153,957,031-153,957,086 , GRCh38.p12 chr3|NT_187533.1: 42,746-42,801 , GRCh38.p12 chr3: 154,239,242-154,239,297 ARHGEF26
    nsv4684995insertion1nstd194human GRCh37 chr3: 153,898,407-153,898,407 , GRCh38.p12 chr3: 154,180,618-154,180,618 , GRCh38.p12 chr3|NT_187533.1: 104,604-104,604 ARHGEF26
    nsv4469801mobile element insertion1nstd166human GRCh37.p13 chr3: 153,963,960-153,963,960 , GRCh38.p12 chr3: 154,246,171-154,246,171 , GRCh38.p12 chr3|NT_187533.1: 35,872-35,872 ARHGEF26
    nsv4469800mobile element insertion1nstd166human GRCh37.p13 chr3: 153,923,731-153,923,731 , GRCh38.p12 chr3|NT_187533.1: 76,101-76,101 , GRCh38.p12 chr3: 154,205,942-154,205,942 ARHGEF26
    nsv4469799mobile element insertion1nstd166human GRCh37.p13 chr3: 153,834,758-153,834,758 , GRCh38.p12 chr3|NT_187533.1: 168,251-168,251 , GRCh38.p12 chr3: 154,116,969-154,116,969 ARHGEF26-AS1
    nsv4469547mobile element insertion1nstd166human GRCh37.p13 chr3: 153,975,519-153,975,519 , GRCh38.p12 chr3: 154,257,730-154,257,730 , GRCh38.p12 chr3|NT_187533.1: 24,313-24,313 , ARHGEF26
    nsv4469546mobile element insertion1nstd166human GRCh37.p13 chr3: 153,876,423-153,876,423 , GRCh38.p12 chr3: 154,158,634-154,158,634 , GRCh38.p12 chr3|NT_187533.1: 126,586-126,586 ARHGEF26
    nsv4469183mobile element insertion1nstd166human GRCh37.p13 chr3: 153,991,564-153,991,564 , GRCh38.p12 chr3: 154,273,775-154,273,775 , GRCh38.p12 chr3|NT_187533.1: 8,268-8,268 DHX36
    nsv4440071insertion1nstd175human GRCh37 chr3: 153,898,408-153,898,408 , GRCh38.p12 chr3: 154,180,619-154,180,619 , GRCh38.p12 chr3|NT_187533.1: 104,603-104,603 ARHGEF26
    nsv4375509copy number variation1nstd173human GRCh37 chr3: 153,819,035-153,910,995 , GRCh38.p12 chr3: 154,101,246-154,193,206 , GRCh38.p12 chr3|NT_187533.1: 88,835-173,649 ARHGEF26-AS1, LOC107987407, 1 more genes
    nsv4374433copy number variation2nstd173human GRCh37 chr3: 153,858,154-153,880,724 , GRCh38.p12 chr3: 154,140,365-154,162,935 , GRCh38.p12 chr3|NT_187533.1: 122,285-144,855 ARHGEF26
    nsv4111196copy number variation1nstd166human GRCh37.p13 chr3: 153,957,448-153,957,528 , GRCh38.p12 chr3: 154,239,659-154,239,739 , GRCh38.p12 chr3|NT_187533.1: 42,304-42,384 ARHGEF26
    nsv4101412copy number variation1nstd166human GRCh37.p13 chr3: 153,899,000-153,911,000 , GRCh38.p12 chr3: 154,181,211-154,193,211 , GRCh38.p12 chr3|NT_187533.1: 88,830-100,840 ARHGEF26
    nsv4100956copy number variation1nstd166human GRCh37.p13 chr3: 153,842,471-153,842,649 , GRCh38.p12 chr3|NT_187533.1: 160,360-160,538 , GRCh38.p12 chr3: 154,124,682-154,124,860 ARHGEF26
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