U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 497

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096583copy number variation1nstd102humanPathogenic GRCh37 chr2: 169,869,772-169,873,319 , GRCh38.p12 chr2: 169,013,262-169,016,809 ABCB11
    nsv7096582copy number variation2nstd102humanUncertain significance GRCh37 chr2: 169,853,125-170,344,644 , GRCh38.p12 chr2: 168,996,615-169,488,134 DHRS9, ABCB11, 3 more genes
    nsv7096382copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 169,783,656-169,783,882 , GRCh38.p12 chr2: 168,927,146-168,927,372 , GRCh38.p12 chr2|NW_003315909.1: 113,773-113,999 ABCB11
    nsv7056492inversion1nstd229human GRCh38 chr2: 168,952,197-168,958,983 , GRCh37.p13 chr2: 169,808,707-169,815,493 ABCB11
    nsv6698060copy number variation1nstd229human GRCh38 chr2: 168,845,584-169,182,309 , GRCh37.p13 chr2: 169,702,094-170,038,819 LRP2, ABCB11, 5 more genes
    nsv6695820copy number variation1nstd229human GRCh38 chr2: 169,029,726-169,030,054 , GRCh37.p13 chr2: 169,886,236-169,886,564 ABCB11
    nsv6686884copy number variation1nstd229human GRCh38 chr2: 168,956,464-168,964,031 , GRCh37.p13 chr2: 169,812,974-169,820,541 ABCB11
    nsv6686261copy number variation1nstd229human GRCh38 chr2: 168,906,610-168,915,217 , GRCh37.p13 chr2: 169,763,120-169,771,727 G6PC2, ABCB11
    nsv6679804copy number variation1nstd229human GRCh38 chr2: 168,985,201-168,996,200 , GRCh37.p13 chr2: 169,841,711-169,852,710 ABCB11
    nsv6678900copy number variation1nstd229human GRCh38 chr2: 168,515,191-170,305,528 , GRCh37.p13 chr2: 169,371,701-171,162,038 METTL5, FASTKD1, 28 more genes
    nsv6627782copy number variation1nstd224human GRCh37 chr2: 169,771,420-169,820,807 , GRCh38.p12 chr2: 168,914,910-168,964,297 ABCB11
    nsv6627781copy number variation1nstd224human GRCh37 chr2: 168,698,913-170,141,066 , GRCh38.p12 chr2: 167,842,403-169,284,556 STK39, CERS6, 17 more genes
    nsv6627281copy number variation1nstd224human GRCh37 chr2: 169,668,122-169,927,200 , GRCh38.p12 chr2: 168,811,612-169,070,690 G6PC2, ABCB11, 3 more genes
    nsv6546083inversion1nstd223human GRCh38 chr2: 168,950,499-168,950,646 , GRCh37.p13 chr2: 169,807,009-169,807,156 ABCB11
    nsv6351862copy number variation1nstd223human GRCh38 chr2: 168,961,701-168,963,300 , GRCh37.p13 chr2: 169,818,211-169,819,810 ABCB11
    nsv6348748copy number variation1nstd223human GRCh38 chr2: 168,938,901-168,939,600 , GRCh37.p13 chr2: 169,795,411-169,796,110 ABCB11
    nsv6348498copy number variation1nstd223human GRCh38 chr2: 169,021,401-169,022,900 , GRCh37.p13 chr2: 169,877,911-169,879,410 ABCB11
    nsv6347882copy number variation1nstd223human GRCh38 chr2: 169,029,726-169,030,038 , GRCh37.p13 chr2: 169,886,236-169,886,548 ABCB11
    nsv6341710copy number variation1nstd223human GRCh38 chr2: 168,997,193-168,998,040 , GRCh37.p13 chr2: 169,853,703-169,854,550 ABCB11
    nsv6340418copy number variation1nstd223human GRCh38 chr2: 168,969,809-168,970,312 , GRCh37.p13 chr2: 169,826,319-169,826,822 ABCB11
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center