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Items: 1 to 20 of 152

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5441024copy number variation1nstd206human GRCh38 chr3: 44,909,778-44,916,620 , GRCh37.p13 chr3: 44,951,270-44,958,112 TGM4, ZDHHC3
    nsv5439590copy number variation1nstd206human GRCh38 chr3: 44,872,653-44,872,718 , GRCh37.p13 chr3: 44,914,145-44,914,210 PPIAP18, TGM4
    nsv5438380copy number variation1nstd206human GRCh38 chr3: 44,914,231-44,915,759 , GRCh37.p13 chr3: 44,955,723-44,957,251 TGM4, ZDHHC3
    nsv5434258copy number variation1nstd206human GRCh38 chr3: 44,872,698-44,872,865 , GRCh37.p13 chr3: 44,914,190-44,914,357 TGM4, PPIAP18
    nsv5074566mobile element insertion1nstd203human GRCh38 chr3: 44,879,370-44,879,370 , GRCh37.p13 chr3: 44,920,862-44,920,862 TGM4
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4924383copy number variation1nstd200human GRCh38 chr3: 44,872,698-44,872,865 , GRCh37.p13 chr3: 44,914,190-44,914,357 PPIAP18, TGM4
    nsv4924382copy number variation1nstd200human GRCh38 chr3: 44,759,215-44,881,079 , GRCh37.p13 chr3: 44,800,707-44,922,571 MIR564, KIF15, 5 more genes
    nsv4911059copy number variation1nstd200human GRCh38 chr3: 44,877,748-44,878,615 , GRCh37.p13 chr3: 44,919,240-44,920,107 TGM4
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4790501copy number variation1nstd200human GRCh37 chr3: 44,919,240-44,920,107 , GRCh38.p12 chr3: 44,877,748-44,878,615 , GRCh38.p12 chr3|NW_009646197.1: 403,098-403,965 TGM4
    nsv4674744copy number variation1nstd102humanUncertain significance GRCh37 chr3: 44,444,902-45,413,927 , GRCh38.p12 chr3: 44,403,410-45,372,435 RPL12P44, TMEM42, 37 more genes
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4521659copy number variation1nstd166human GRCh37.p13 chr3: 44,955,748-44,957,196 , GRCh38.p12 chr3: 44,914,256-44,915,704 , GRCh38.p12 chr3|NW_009646197.1: 439,606-441,054 TGM4, ZDHHC3
    nsv4470640mobile element insertion1nstd166human GRCh37.p13 chr3: 44,956,124-44,956,124 , GRCh38.p12 chr3: 44,914,632-44,914,632 , GRCh38.p12 chr3|NW_009646197.1: 439,982-439,982 ZDHHC3, TGM4
    nsv4087795copy number variation1nstd166human GRCh37.p13 chr3: 44,923,886-44,926,964 , GRCh38.p12 chr3|NW_009646197.1: 407,744-410,822 , GRCh38.p12 chr3: 44,882,394-44,885,472 TGM4
    nsv4085755copy number variation1nstd166human GRCh37.p13 chr3: 44,931,929-44,932,712 , GRCh38.p12 chr3|NW_009646197.1: 415,787-416,570 , GRCh38.p12 chr3: 44,890,437-44,891,220 TGM4
    nsv4084488copy number variation1nstd166human GRCh37.p13 chr3: 44,939,759-44,942,678 , GRCh38.p12 chr3: 44,898,267-44,901,186 , GRCh38.p12 chr3|NW_009646197.1: 423,617-426,536 TGM4
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