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  • The following terms were not found in dbVar: Fmoc, Trifluoromethyl, homophenylalanine.
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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5575125copy number variation1nstd207human GRCh38 chr2: 44,239,968-44,241,691 , GRCh37.p13 chr2: 44,467,107-44,468,830 PPM1B
    nsv5570786copy number variation1nstd207human GRCh38 chr2: 26,275,190-26,275,273 , GRCh37.p13 chr2: 26,498,058-26,498,141 HADHB
    nsv4092237copy number variation1nstd166human GRCh37.p13 chr2: 172,031,492-172,044,431 , GRCh38.p12 chr2: 171,174,982-171,187,921 TLK1
    nsv4085525copy number variation1nstd166human GRCh37.p13 chr2: 171,960,940-171,969,575 , GRCh38.p12 chr2: 171,104,430-171,113,065 TLK1
    nsv4061425copy number variation1nstd166human GRCh37.p13 chr2: 44,415,545-44,422,332 , GRCh38.p12 chr2: 44,188,406-44,195,193 PPM1B
    nsv4065310copy number variation1nstd166human GRCh37.p13 chr2: 26,471,840-26,476,596 , GRCh38.p12 chr2: 26,248,972-26,253,728 HADHB
    nsv4077865copy number variation1nstd166human GRCh37.p13 chr2: 171,929,277-171,932,706 , GRCh38.p12 chr2: 171,072,767-171,076,196 TLK1
    nsv4057135copy number variation1nstd166human GRCh37.p13 chr2: 44,459,673-44,461,994 , GRCh38.p12 chr2: 44,232,534-44,234,855 PPM1B
    nsv4087762copy number variation1nstd166human GRCh37.p13 chr2: 171,999,980-172,001,713 , GRCh38.p12 chr2: 171,143,470-171,145,203 TLK1
    nsv4059884copy number variation1nstd166human GRCh37.p13 chr2: 44,467,109-44,468,831 , GRCh38.p12 chr2: 44,239,970-44,241,692 PPM1B
    nsv4082677copy number variation1nstd166human GRCh37.p13 chr2: 172,084,934-172,085,906 , GRCh38.p12 chr2: 171,228,424-171,229,396 TLK1
    nsv4087598copy number variation1nstd166human GRCh37.p13 chr2: 171,973,066-171,973,624 , GRCh38.p12 chr2: 171,116,556-171,117,114 TLK1
    nsv4518818copy number variation1nstd166human GRCh37.p13 chr2: 172,022,287-172,022,583 , GRCh38.p12 chr2: 171,165,777-171,166,073 TLK1
    nsv4070231copy number variation1nstd166human GRCh37.p13 chr2: 44,424,023-44,424,282 , GRCh38.p12 chr2: 44,196,884-44,197,143 PPM1B
    nsv4087333copy number variation1nstd166human GRCh37.p13 chr2: 172,062,182-172,062,250 , GRCh38.p12 chr2: 171,205,672-171,205,740 TLK1
    nsv4091682copy number variation1nstd166human GRCh37.p13 chr2: 171,912,712-171,912,776 , GRCh38.p12 chr2: 171,056,202-171,056,266 TLK1
    nsv4081884copy number variation1nstd166human GRCh37.p13 chr2: 171,897,815-171,897,875 , GRCh38.p12 chr2: 171,041,305-171,041,365 TLK1
    nsv4078872copy number variation1nstd166human GRCh37.p13 chr2: 172,036,561-172,036,618 , GRCh38.p12 chr2: 171,180,051-171,180,108 TLK1
    nsv4059876copy number variation1nstd166human GRCh37.p13 chr2: 103,038,442-103,038,494 , GRCh38.p12 chr2: 102,421,982-102,422,034 IL18RAP
    nsv4085759copy number variation1nstd166human GRCh37.p13 chr2: 171,914,057-171,914,108 , GRCh38.p12 chr2: 171,057,547-171,057,598 TLK1
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