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 137

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097553copy number variation1nstd102humanPathogenic GRCh37 chr5: 94,800,311-96,107,383 , GRCh38.p12 chr5: 95,464,607-96,771,679 LOC105379675, GPR150, 27 more genes
    nsv7058036inversion1nstd229human GRCh38 chr5: 94,195,543-97,660,538 , GRCh37.p13 chr5: 93,531,248-96,996,242 RIOK2, SPATA9, 51 more genes
    nsv7044198inversion1nstd229human GRCh38 chr5: 93,856,097-99,790,151 , GRCh37.p13 chr5: 93,191,803-99,125,855 FAM81B, LOC107986365, 78 more genes
    nsv6773004copy number variation1nstd229human GRCh38 chr5: 94,767,305-97,708,544 , GRCh37.p13 chr5: 94,103,010-97,044,248 FABP5P5, SPATA9, 45 more genes
    nsv6770732copy number variation1nstd229human GRCh38 chr5: 95,768,680-95,951,039 , GRCh37.p13 chr5: 95,104,384-95,286,743 LOC105379091, GLRX, 6 more genes
    nsv6767196copy number variation1nstd229human GRCh38 chr5: 95,464,994-96,106,661 , GRCh37.p13 chr5: 94,800,698-95,442,365 ELL2, ARSK, 19 more genes
    nsv6630453copy number variation1nstd224human GRCh37 chr5: 95,072,623-95,423,944 , GRCh38.p12 chr5: 95,736,919-96,088,240 GLRX, LINC01554, 11 more genes
    nsv6410812copy number variation1nstd223human GRCh38 chr5: 95,381,684-95,927,497 , GRCh37.p13 chr5: 94,717,388-95,263,201 SKIC3, ARSK, 17 more genes
    nsv6405135copy number variation1nstd223human GRCh38 chr5: 95,768,680-95,951,039 , GRCh37.p13 chr5: 95,104,384-95,286,743 LOC105379091, LINC01554, 6 more genes
    nsv6313580copy number variation1nstd102humanPathogenic GRCh37 chr5: 93,650,000-114,969,108 , GRCh38.p12 chr5: 94,314,295-115,633,411 FER, HMGN1P15, 222 more genes
    nsv6135443copy number variation1nstd213human GRCh37 chr5: 94,660,000-95,520,001 , GRCh38.p12 chr5: 95,324,296-96,184,297 FAM81B, FABP5P5, 23 more genes
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv5033775inversion1nstd200human GRCh38 chr5: 76,373,686-102,541,075 , GRCh37.p13 chr5: 75,669,511-101,876,779 , F2RL1, 331 more genes
    nsv4947258copy number variation1nstd200human GRCh38 chr5: 95,817,297-95,819,724 , GRCh37.p13 chr5: 95,153,001-95,155,428 GLRX
    nsv4947257copy number variation1nstd200human GRCh38 chr5: 95,806,009-95,814,048 , GRCh37.p13 chr5: 95,141,713-95,149,752 GLRX
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4675889copy number variation1nstd102humanUncertain significance GRCh37 chr5: 94,715,085-95,251,238 , GRCh38.p12 chr5: 95,379,381-95,915,534 RHOBTB3, ELL2, 17 more genes
    nsv4675667copy number variation1nstd102humanPathogenic GRCh37 chr5: 72,790,061-97,478,870 , GRCh38.p12 chr5: 73,494,236-98,143,166 LOC101929380, LIX1-AS1, 318 more genes
    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