U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 29

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093621copy number variation1nstd102humanPathogenic GRCh37 chr10: 100,453,637-100,481,605 , GRCh38.p12 chr10: 98,693,880-98,721,848 HPSE2
    nsv7093622copy number variation1nstd102humanPathogenic GRCh37 chr10: 100,481,394-100,503,833 , GRCh38.p12 chr10: 98,721,637-98,744,076 HPSE2
    nsv3905075copy number variation1nstd102humanBenign GRCh37 chr10: 100,703,088-100,742,391 , GRCh38.p12 chr10: 98,943,331-98,982,634 HPSE2
    nsv3902857copy number variation1nstd102humanBenign GRCh37 chr10: 100,688,825-100,704,597 , GRCh38.p12 chr10: 98,929,068-98,944,840 HPSE2
    nsv6309050copy number variation1nstd102humanUncertain significance GRCh37 chr10: 100,903,975-100,904,176 , GRCh38.p12 chr10: 99,144,218-99,144,419 HPSE2
    nsv3922175copy number variation1nstd102humanBenign GRCh38 chr10: 98,907,968-98,937,040 , GRCh37 chr10: 100,667,725-100,696,797 , NCBI36 chr10: 100,657,715-100,686,787 HPSE2, MIR6507
    nsv3909051copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr10: 100,690,060-100,911,811 , GRCh38.p12 chr10: 98,930,303-99,152,054 HPSE2, ARL5AP2, 1 more genes
    nsv3893895copy number variation1nstd102humanBenign GRCh37 chr10: 100,734,484-100,830,309 , GRCh38.p12 chr10: 98,974,727-99,070,552 HPSE2, RPL7P36, 1 more genes
    nsv6637175copy number variation1nstd102humanUncertain significance GRCh37 chr10: 100,495,923-101,002,224 , GRCh38.p12 chr10: 98,736,166-99,242,467 HPSE2, MIR6507, 2 more genes
    nsv4456005copy number variation1nstd102humanPathogenic GRCh37 chr10: 100,067,156-100,257,755 , GRCh38.p12 chr10: 98,307,399-98,497,998 HPSE2, HPS1, 5 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 HPSE2, RNU7-12P, 1876 more genes
    nsv3920295copy number variation1nstd102humanPathogenic NCBI36 chr10: 81,675,342-135,374,737 , GRCh37.p13 chr10: 81,685,362-135,524,747 , GRCh38.p12 chr10: 79,925,606-133,787,422 HPSE2, EIF2S2P3, 895 more genes
    nsv3911437copy number variation1nstd102humanPathogenic GRCh38 chr10: 93,181,201-101,356,779 , NCBI36 chr10: 94,930,948-103,106,526 , GRCh37 chr10: 94,940,958-103,116,536 HPSE2, SLF2, 171 more genes
    nsv3894877copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,908,171-101,809,723 , GRCh38.p12 chr10: 92,148,414-100,049,966 HPSE2, RNY3P12, 146 more genes
    nsv6309049copy number variation1nstd102humanPathogenic GRCh37 chr10: 100,177,321-101,611,388 , GRCh38.p12 chr10: 98,417,564-99,851,631 HPSE2, SLC25A28, 18 more genes
    nsv3906389copy number variation1nstd102humanPathogenic GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996 HPSE2, LOC100419870, 2105 more genes
    nsv3891157copy number variation1nstd102humanPathogenic GRCh37 chr10: 98,087-135,477,883 , GRCh38.p12 chr10: 52,147-133,740,558 HPSE2, AGAP14P, 2097 more genes
    nsv3902271copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639 HPSE2, ANXA11, 2085 more genes
    nsv3891958copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,297-135,378,918 , GRCh38.p12 chr10: 47,357-133,565,414 HPSE2, TUBB8, 2085 more genes
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 HPSE2, EXOC6, 1906 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    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