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 414

    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
    nsv5886416copy number variation1nstd209human GRCh38 chrX: 87,626,840-87,626,961 , GRCh37.p13 chrX: 86,881,840-86,881,961 KLHL4
    nsv5720215mobile element insertion1nstd211human GRCh38 chrX: 87,663,439-87,663,439 , GRCh37.p13 chrX: 86,918,439-86,918,439 KLHL4
    nsv5605679insertion1nstd207human GRCh38 chrX: 87,663,423-87,663,423 , GRCh37.p13 chrX: 86,918,423-86,918,423 KLHL4
    nsv5557239mobile element insertion1nstd206human GRCh38 chrX: 87,663,439-87,663,490 , GRCh37.p13 chrX: 86,918,439-86,918,490 KLHL4
    nsv5543775insertion1nstd206human GRCh38 chrX: 87,538,090-87,538,090 , GRCh37.p13 chrX: 86,793,093-86,793,093 KLHL4
    nsv5362400translocation1nstd200human GRCh38 chr5: 90,155,064-90,155,064 , GRCh38 chrX: 87,657,123-87,657,123 , GRCh37.p13 chr5: 89,450,881-89,450,881 , GRCh37.p13 chrX: 86,912,123-86,912,123 KLHL4
    nsv5195392mobile element insertion1nstd203human GRCh38 chrX: 87,545,232-87,545,244 , GRCh37.p13 chrX: 86,800,235-86,800,247 KLHL4
    nsv5174347mobile element insertion1nstd203human GRCh38 chrX: 87,611,078-87,611,095 , GRCh37.p13 chrX: 86,866,081-86,866,098 KLHL4
    nsv5059979copy number variation1nstd102humanPathogenic GRCh37 chrX: 56,469,080-155,233,731 , GRCh38.p12 chrX: 56,442,647-156,004,066 VDAC1P1, LOC105373299, 1364 more genes
    nsv5030775inversion1nstd200human GRCh38 chrX: 23,472,124-121,561,941 , GRCh37.p13 chrX: 23,490,241-120,695,795 , GPR173, 1350 more genes
    nsv4908539copy number variation1nstd200human GRCh38 chrX: 87,647,700-87,648,337 , GRCh37.p13 chrX: 86,902,700-86,903,337 KLHL4
    nsv4908538copy number variation1nstd200human GRCh38 chrX: 87,597,519-87,607,656 , GRCh37.p13 chrX: 86,852,522-86,862,659 KLHL4
    nsv4908537copy number variation1nstd200human GRCh38 chrX: 87,530,129-87,531,272 , GRCh37.p13 chrX: 86,785,132-86,786,275 KLHL4
    nsv4905725copy number variation1nstd200human GRCh38 chrX: 87,659,355-87,659,564 , GRCh37.p13 chrX: 86,914,355-86,914,564 KLHL4
    nsv4905724copy number variation1nstd200human GRCh38 chrX: 87,593,220-87,596,487 , GRCh37.p13 chrX: 86,848,223-86,851,490 KLHL4
    nsv4905721copy number variation1nstd200human GRCh38 chrX: 87,262,205-87,662,069 , GRCh37.p13 chrX: 86,517,208-86,917,069 KLHL4
    nsv4771781copy number variation1nstd200human GRCh37 chrX: 86,902,700-86,903,337 , GRCh38.p12 chrX: 87,647,700-87,648,337 KLHL4
    nsv4771780copy number variation1nstd200human GRCh37 chrX: 86,895,471-86,897,850 , GRCh38.p12 chrX: 87,640,471-87,642,850 KLHL4
    nsv4771779copy number variation1nstd200human GRCh37 chrX: 86,894,247-86,896,060 , GRCh38.p12 chrX: 87,639,247-87,641,060 KLHL4
    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