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 650

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5973780inversion1nstd209human GRCh38 chrX: 19,843,181-19,843,729 , GRCh37.p13 chrX: 19,861,299-19,861,847 SH3KBP1
    nsv5882150copy number variation1nstd209human GRCh38 chrX: 19,595,507-19,595,600 , GRCh37.p13 chrX: 19,613,625-19,613,718 SH3KBP1
    nsv5881285copy number variation1nstd209human GRCh38 chrX: 19,554,006-19,554,072 , GRCh37.p13 chrX: 19,572,124-19,572,190 SH3KBP1
    nsv5879513copy number variation1nstd209human GRCh38 chrX: 19,776,970-19,777,586 , GRCh37.p13 chrX: 19,795,088-19,795,704 SH3KBP1
    nsv5879206copy number variation1nstd209human GRCh38 chrX: 19,811,183-19,813,084 , GRCh37.p13 chrX: 19,829,301-19,831,202 SH3KBP1
    nsv5868201copy number variation1nstd209human GRCh38 chrX: 19,618,709-19,619,008 , GRCh37.p13 chrX: 19,636,827-19,637,126 SH3KBP1
    nsv5722085mobile element insertion1nstd211human GRCh38 chrX: 19,611,978-19,611,978 , GRCh37.p13 chrX: 19,630,096-19,630,096 SH3KBP1
    nsv5715551mobile element insertion1nstd211human GRCh38 chrX: 19,791,790-19,791,790 , GRCh37.p13 chrX: 19,809,908-19,809,908 SH3KBP1
    nsv5670901copy number variation1nstd207human GRCh38 chrX: 19,554,006-19,554,072 , GRCh37.p13 chrX: 19,572,124-19,572,190 SH3KBP1
    nsv5669008copy number variation1nstd207human GRCh38 chrX: 19,811,183-19,813,084 , GRCh37.p13 chrX: 19,829,301-19,831,202 SH3KBP1
    nsv5665479copy number variation1nstd207human GRCh38 chrX: 19,842,556-19,843,180 , GRCh37.p13 chrX: 19,860,674-19,861,298 SH3KBP1
    nsv5619924insertion1nstd207human GRCh38 chrX: 19,730,387-19,730,387 , GRCh37.p13 chrX: 19,748,505-19,748,505 SH3KBP1
    nsv5618254insertion1nstd207human GRCh38 chrX: 19,727,710-19,727,710 , GRCh37.p13 chrX: 19,745,828-19,745,828 SH3KBP1
    nsv5612816insertion1nstd207human GRCh38 chrX: 19,761,271-19,761,271 , GRCh37.p13 chrX: 19,779,389-19,779,389 SH3KBP1
    nsv5612115insertion1nstd207human GRCh38 chrX: 19,572,194-19,572,194 , GRCh37.p13 chrX: 19,590,312-19,590,312 SH3KBP1
    nsv5553504inversion1nstd206human GRCh38 chrX: 19,842,432-19,843,181 , GRCh37.p13 chrX: 19,860,550-19,861,299 SH3KBP1
    nsv5427549copy number variation1nstd206human GRCh38 chrX: 19,811,185-19,813,085 , GRCh37.p13 chrX: 19,829,303-19,831,203 SH3KBP1
    nsv5427257copy number variation1nstd206human GRCh38 chrX: 19,888,000-19,888,347 , GRCh37.p13 chrX: 19,906,118-19,906,465 SH3KBP1
    nsv5424717copy number variation1nstd206human GRCh38 chrX: 19,617,196-19,617,503 , GRCh37.p13 chrX: 19,635,314-19,635,621 SH3KBP1
    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