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 332

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075861inversion1nstd229human GRCh38 chr21: 32,596,447-36,013,453 , GRCh37.p13 chr21: 33,968,757-37,385,751 , IFNAR2, 64 more genes
    nsv7070554inversion1nstd229human GRCh38 chr21: 28,138,154-35,660,050 , GRCh37.p13 chr21: 29,510,473-37,032,348 , OR7E23P, 160 more genes
    nsv7070253inversion1nstd229human GRCh38 chr21: 28,377,443-35,730,342 , GRCh37.p13 chr21: 29,749,764-37,102,640 , HUNK, 161 more genes
    nsv6627152copy number variation1nstd224human GRCh37 chr21: 35,726,226-35,911,599 , GRCh38.p12 chr21: 34,353,927-34,539,301 RCAN1, KCNE1, 6 more genes
    nsv6627005copy number variation6nstd224human GRCh37 chr21: 35,726,226-35,895,986 , GRCh38.p12 chr21: 34,353,927-34,523,688 RCAN1, KCNE1, 6 more genes
    nsv6627004copy number variation1nstd224human GRCh37 chr21: 35,726,226-35,893,737 , GRCh38.p12 chr21: 34,353,927-34,521,439 RCAN1, KCNE1, 6 more genes
    nsv6626872copy number variation1nstd224human GRCh37 chr21: 35,722,817-35,904,483 , GRCh38.p12 chr21: 34,350,518-34,532,185 RCAN1, KCNE1, 6 more genes
    nsv6626871copy number variation2nstd224human GRCh37 chr21: 35,722,817-35,903,830 , GRCh38.p12 chr21: 34,350,518-34,531,532 RCAN1, KCNE1, 6 more genes
    nsv6626642copy number variation1nstd224human GRCh37 chr21: 35,736,166-35,907,413 , GRCh38.p12 chr21: 34,363,867-34,535,115 RCAN1, KCNE1, 6 more genes
    nsv6626624copy number variation1nstd224human GRCh37 chr21: 1-48,129,895 , GRCh38.p12 chr21: 8,522,361-46,699,983 , ATP5PO, 657 more genes
    nsv6596327inversion1nstd223human GRCh38 chr21: 28,377,391-35,730,332 , GRCh37.p13 chr21: 29,749,712-37,102,630 , LOC107985515, 161 more genes
    nsv6315551copy number variation1nstd102humanPathogenic GRCh37 chr21: 14,420,615-48,080,926 , GRCh38.p12 chr21: 13,048,294-46,661,014 LTN1, LOC105372740, 622 more genes
    nsv6314196copy number variation1nstd102humanUncertain significance GRCh37 chr21: 27,185,913-35,853,445 , GRCh38.p12 chr21: 25,813,602-34,481,147 RPL12P9, CLDN17, 173 more genes
    nsv6313951copy number variation1nstd102humanPathogenic GRCh37 chr21: 15,041,209-48,097,372 , GRCh38.p12 chr21: 13,668,888-46,677,460 LOC107985515, ATP5PF, 606 more genes
    nsv6311248copy number variation2nstd102humanUncertain significance GRCh37 chr21: 32,439,271-39,212,984 , GRCh38.p12 chr21: 31,066,952-37,840,682 ATP5PO, LOC105372789, 131 more genes
    nsv6311105copy number variation2nstd102humanUncertain significance GRCh37 chr21: 35,742,778-35,821,932 , GRCh38.p12 chr21: 34,370,479-34,449,634 SMIM34, SMIM11, 5 more genes
    nsv6307475copy number variation1nstd186human GRCh37 chr21: 35,748,107-35,866,106 , GRCh38.p12 chr21: 34,375,808-34,493,808 KCNE1, SMIM11, 4 more genes
    nsv6289996copy number variation1nstd102humanPathogenic GRCh37 chr21: 1-48,129,895 , GRCh38.p12 chr21: 8,522,361-46,699,983 KRTAP7-1, MAP3K7CL, 656 more genes
    nsv6146954copy number variation1nstd206human GRCh38 chr21: 34,375,808-34,493,808 , GRCh37.p13 chr21: 35,748,107-35,866,106 KCNE1, SMIM11, 4 more genes
    nsv6134054copy number variation1nstd213human GRCh37 chr21: 15,200,000-37,410,001 , GRCh38.p12 chr21: 13,827,679-36,037,703 , ATP5PF, 320 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