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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6115702copy number variation1nstd186human GRCh37 chrX: 131,921,185-131,921,581 , GRCh38.p12 chrX: 132,787,157-132,787,553 HS6ST2
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5969005copy number variation1nstd209human GRCh38 chrX: 132,805,379-132,807,578 , GRCh37.p13 chrX: 131,939,407-131,941,606 HS6ST2
    nsv5884934copy number variation1nstd209human GRCh38 chrX: 132,805,403-132,807,513 , GRCh37.p13 chrX: 131,939,431-131,941,541 HS6ST2
    nsv5877301copy number variation1nstd209human GRCh38 chrX: 132,779,678-132,780,299 , GRCh37.p13 chrX: 131,913,706-131,914,327 HS6ST2
    nsv5871709copy number variation1nstd209human GRCh38 chrX: 132,851,324-132,853,702 , GRCh37.p13 chrX: 131,985,352-131,987,730 HS6ST2
    nsv5729623mobile element insertion1nstd211human GRCh38 chrX: 132,879,310-132,879,310 , GRCh37.p13 chrX: 132,013,338-132,013,338 HS6ST2
    nsv5727681mobile element insertion2nstd211human GRCh38 chrX: 132,818,712-132,818,712 , GRCh37.p13 chrX: 131,952,740-131,952,740 HS6ST2
    nsv5724793mobile element insertion1nstd211human GRCh38 chrX: 132,712,508-132,712,508 , GRCh37.p13 chrX: 131,846,536-131,846,536 HS6ST2
    nsv5722372mobile element insertion1nstd211human GRCh38 chrX: 132,648,990-132,648,990 , GRCh37.p13 chrX: 131,783,018-131,783,018 HS6ST2
    nsv5719539mobile element insertion1nstd211human GRCh38 chrX: 132,908,962-132,908,962 , GRCh37.p13 chrX: 132,042,990-132,042,990 HS6ST2, NAA20P1
    nsv5670488copy number variation1nstd207human GRCh38 chrX: 132,805,403-132,807,513 , GRCh37.p13 chrX: 131,939,431-131,941,541 HS6ST2
    nsv5611224insertion1nstd207human GRCh38 chrX: 132,637,929-132,637,929 , GRCh37.p13 chrX: 131,771,957-131,771,957 HS6ST2
    nsv5561449mobile element insertion1nstd206human GRCh38 chrX: 132,712,508-132,712,559 , GRCh37.p13 chrX: 131,846,536-131,846,587 HS6ST2
    nsv5559097mobile element insertion1nstd206human GRCh38 chrX: 132,648,990-132,649,041 , GRCh37.p13 chrX: 131,783,018-131,783,069 HS6ST2
    nsv5557939mobile element insertion1nstd206human GRCh38 chrX: 132,818,712-132,818,763 , GRCh37.p13 chrX: 131,952,740-131,952,791 HS6ST2
    nsv5554528mobile element insertion1nstd206human GRCh38 chrX: 132,879,310-132,879,361 , GRCh37.p13 chrX: 132,013,338-132,013,389 HS6ST2
    nsv5551569insertion1nstd206human GRCh38 chrX: 132,721,879-132,721,879 , GRCh37.p13 chrX: 131,855,907-131,855,907 HS6ST2
    nsv5433417copy number variation1nstd206human GRCh38 chrX: 132,787,157-132,787,553 , GRCh37.p13 chrX: 131,921,185-131,921,581 HS6ST2
    nsv5432724copy number variation1nstd206human GRCh38 chrX: 132,851,381-132,852,345 , GRCh37.p13 chrX: 131,985,409-131,986,373 HS6ST2
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