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 177

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5706705mobile element insertion1nstd211human GRCh38 chr9: 99,122,954-99,122,954 , GRCh37.p13 chr9: 101,885,236-101,885,236 TGFBR1
    nsv5547044insertion1nstd206human GRCh38 chr9: 99,131,718-99,131,768 , GRCh37.p13 chr9: 101,894,000-101,894,050 TGFBR1
    nsv5381561copy number variation1nstd102humanPathogenic GRCh37 chr9: 97,834,573-107,199,088 , GRCh38.p12 chr9: 95,072,291-104,436,807 TBC1D2, ZNF782, 170 more genes
    nsv5381484copy number variation1nstd102humanUncertain significance GRCh37 chr9: 101,900,318-101,903,694 , GRCh38.p12 chr9: 99,138,036-99,141,412 TGFBR1
    nsv4982741copy number variation1nstd200human GRCh38 chr9: 99,130,795-99,131,308 , GRCh37.p13 chr9: 101,893,077-101,893,590 TGFBR1
    nsv4982740copy number variation1nstd200human GRCh38 chr9: 99,111,209-99,111,338 , GRCh37.p13 chr9: 101,873,491-101,873,620 TGFBR1
    nsv4982739copy number variation1nstd200human GRCh38 chr9: 99,107,756-99,108,001 , GRCh37.p13 chr9: 101,870,038-101,870,283 TGFBR1
    nsv4982738copy number variation1nstd200human GRCh38 chr9: 99,097,032-99,102,517 , GRCh37.p13 chr9: 101,859,314-101,864,799 TGFBR1
    nsv4824210copy number variation1nstd200human GRCh37 chr9: 101,893,077-101,893,590 , GRCh38.p12 chr9: 99,130,795-99,131,308 TGFBR1
    nsv4824209copy number variation1nstd200human GRCh37 chr9: 101,886,883-101,887,273 , GRCh38.p12 chr9: 99,124,601-99,124,991 TGFBR1
    nsv4824208copy number variation1nstd200human GRCh37 chr9: 101,873,491-101,873,620 , GRCh38.p12 chr9: 99,111,209-99,111,338 TGFBR1
    nsv4824207copy number variation1nstd200human GRCh37 chr9: 101,859,314-101,864,799 , GRCh38.p12 chr9: 99,097,032-99,102,517 TGFBR1
    nsv4684256copy number variation1nstd102humanPathogenic GRCh37 chr9: 96,126,075-108,535,272 , GRCh38.p12 chr9: 93,363,793-105,772,991 RPS26P37, MIR27B, 238 more genes
    nsv4683731copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 101,904,808-101,912,471 , GRCh38.p12 chr9: 99,142,526-99,150,189 TGFBR1, RNA5SP290
    nsv4675547copy number variation1nstd102humanUncertain significance GRCh37 chr9: 100,953,443-102,003,384 , GRCh38.p12 chr9: 98,191,161-99,241,102 SEC61B, TBC1D2, 15 more genes
    nsv4614567copy number variation1nstd183human GRCh37 chr9: 101,910,180-101,913,923 , GRCh38.p12 chr9: 99,147,898-99,151,641 TGFBR1
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4455496copy number variation1nstd102humanPathogenic GRCh37 chr9: 101,878,960-101,949,121 , GRCh38.p12 chr9: 99,116,678-99,186,839 RNA5SP290, TGFBR1, 2 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
    nsv4454212copy number variation1nstd102humanPathogenic GRCh38 chr9: 99,105,186-99,105,322 , GRCh37 chr9: 101,867,468-101,867,604 TGFBR1
    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