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 308

    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
    nsv5976870copy number variation1nstd209human GRCh38 chrX: 131,756,897-131,795,157 , GRCh37.p13 chrX: 130,890,925-130,929,185 MCRIP2P1, FIRRE
    nsv5954003insertion1nstd209human GRCh38 chrX: 131,795,356-131,795,356 , GRCh37.p13 chrX: 130,929,384-130,929,384 MCRIP2P1, FIRRE
    nsv5878163copy number variation1nstd209human GRCh38 chrX: 131,348,092-131,861,518 , GRCh37.p13 chrX: 130,482,066-130,995,546 HDGFP1, OR1AA1P, 12 more genes
    nsv5555995sequence alteration1nstd206human GRCh38 chrX: 131,678,316-131,841,115 , GRCh37.p13 chrX: 130,812,329-130,975,143 FIRRE, PNKDP1, 1 more genes
    nsv5433837copy number variation1nstd206human GRCh38 chrX: 131,645,648-131,835,198 , GRCh37.p13 chrX: 130,779,657-130,969,226 FIRRE, HDGFP1, 2 more genes
    nsv5414094copy number variation1nstd206human GRCh38 chrX: 131,334,000-131,840,381 , GRCh37.p13 chrX: 130,467,974-130,974,409 LOC102723546, OR13H1, 13 more genes
    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
    nsv4909147copy number variation1nstd200human GRCh38 chrX: 131,795,230-131,875,059 , GRCh37.p13 chrX: 130,929,258-131,009,087 PNKDP1, FIRRE, 1 more genes
    nsv4909143copy number variation1nstd200human GRCh38 chrX: 131,518,601-131,935,134 , GRCh37.p13 chrX: 130,652,575-131,069,162 OR2AF1P, FIRRE, 6 more genes
    nsv4909142copy number variation1nstd200human GRCh38 chrX: 131,512,551-131,811,922 , GRCh37.p13 chrX: 130,646,525-130,945,950 OR2AF1P, FIRRE, 6 more genes
    nsv4909140copy number variation1nstd200human GRCh38 chrX: 131,469,391-131,995,434 , GRCh37.p13 chrX: 130,603,365-131,129,462 FIRRE, NLRP7P1, 8 more genes
    nsv4782345copy number variation1nstd200human GRCh37 chrX: 130,929,258-131,009,087 , GRCh38.p12 chrX: 131,795,230-131,875,059 MCRIP2P1, FIRRE, 1 more genes
    nsv4782340copy number variation1nstd200human GRCh37 chrX: 130,646,525-130,945,950 , GRCh38.p12 chrX: 131,512,551-131,811,922 OR7L1P, HDGFP1, 6 more genes
    nsv4782339copy number variation1nstd200human GRCh37 chrX: 130,603,365-131,129,462 , GRCh38.p12 chrX: 131,469,391-131,995,434 RNA5SP514, OR7L1P, 8 more genes
    nsv4769250copy number variation1nstd201human GRCh37 chrX: 96,096,220-155,208,244 , GRCh38.p12 chrX: 96,841,221-155,978,579 , AGTR2, 959 more genes
    nsv4769249copy number variation1nstd201human GRCh37 chrX: 61,728,816-155,233,846 , GRCh38.p12 chrX: 62,509,346-156,004,181 , ABCB7, 1364 more genes
    nsv4728654copy number variation1nstd102humanLikely benign GRCh37 chrX: 130,809,978-131,200,553 , GRCh38.p12 chrX: 131,675,965-132,066,525 RNA5SP514, STK26, 3 more genes
    nsv4728533copy number variation1nstd102humanPathogenic GRCh37 chrX: 94,264,404-155,233,731 , GRCh38.p12 chrX: 95,009,405-156,004,066 CT45A10, MIR224, 968 more genes
    nsv4728499copy number variation1nstd102humanPathogenic GRCh37 chrX: 55,507,789-155,198,481 , GRCh38.p12 chrX: 55,481,356-155,968,816 GABRE, RN7SL325P, 1371 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