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Items: 1 to 20 of 306

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7045068inversion1nstd229human GRCh38 chr4: 138,588,072-141,319,129 , GRCh37.p13 chr4: 139,509,226-142,240,283 RN7SKP253, FTH1P24, 41 more genes
    nsv6754860copy number variation1nstd229human GRCh38 chr4: 138,969,881-139,071,149 , GRCh37.p13 chr4: 139,891,035-139,992,303 RNU6-531P, ELF2, 2 more genes
    nsv6750580copy number variation1nstd229human GRCh38 chr4: 139,010,391-139,049,486 , GRCh37.p13 chr4: 139,931,545-139,970,640 NOCT, LOC105377448
    nsv6747471copy number variation1nstd229human GRCh38 chr4: 138,808,101-139,054,800 , GRCh37.p13 chr4: 139,729,255-139,975,954 LOC105377448, RNU6-531P, 1 more genes
    nsv6747065copy number variation1nstd229human GRCh38 chr4: 139,032,247-139,037,371 , GRCh37.p13 chr4: 139,953,401-139,958,525 NOCT
    nsv6745845copy number variation1nstd229human GRCh38 chr4: 138,824,101-139,071,800 , GRCh37.p13 chr4: 139,745,255-139,992,954 RNU6-531P, NOCT, 2 more genes
    nsv6744898copy number variation1nstd229human GRCh38 chr4: 139,026,860-139,027,179 , GRCh37.p13 chr4: 139,948,014-139,948,333 NOCT
    nsv6744374copy number variation1nstd229human GRCh38 chr4: 138,539,299-139,033,525 , GRCh37.p13 chr4: 139,460,453-139,954,679 LOC105377448, NOCT, 1 more genes
    nsv6743555copy number variation1nstd229human GRCh38 chr4: 138,946,701-139,054,400 , GRCh37.p13 chr4: 139,867,855-139,975,554 LOC105377448, NOCT, 1 more genes
    nsv6742929copy number variation1nstd229human GRCh38 chr4: 138,831,146-139,064,807 , GRCh37.p13 chr4: 139,752,300-139,985,961 ELF2, LOC105377448, 2 more genes
    nsv6741333copy number variation1nstd229human GRCh38 chr4: 139,020,637-139,041,534 , GRCh37.p13 chr4: 139,941,791-139,962,688 NOCT
    nsv6740712copy number variation1nstd229human GRCh38 chr4: 139,011,401-139,019,424 , GRCh37.p13 chr4: 139,932,555-139,940,578 NOCT, LOC105377448
    nsv6738689copy number variation1nstd229human GRCh38 chr4: 139,030,475-139,035,390 , GRCh37.p13 chr4: 139,951,629-139,956,544 NOCT
    nsv6572116inversion1nstd223human GRCh38 chr4: 139,042,112-139,042,671 , GRCh37.p13 chr4: 139,963,266-139,963,825 NOCT
    nsv6565066inversion1nstd223human GRCh38 chr4: 139,017,249-139,017,653 , GRCh37.p13 chr4: 139,938,403-139,938,807 NOCT
    nsv6392393copy number variation1nstd223human GRCh38 chr4: 139,027,573-139,031,156 , GRCh37.p13 chr4: 139,948,727-139,952,310 NOCT
    nsv6391609copy number variation1nstd223human GRCh38 chr4: 139,015,301-139,017,500 , GRCh37.p13 chr4: 139,936,455-139,938,654 NOCT
    nsv6391572copy number variation1nstd223human GRCh38 chr4: 139,046,220-139,047,915 , GRCh37.p13 chr4: 139,967,374-139,969,069 NOCT
    nsv6391141copy number variation1nstd223human GRCh38 chr4: 139,021,301-139,021,900 , GRCh37.p13 chr4: 139,942,455-139,943,054 NOCT
    nsv6390187copy number variation1nstd223human GRCh38 chr4: 139,045,693-139,046,748 , GRCh37.p13 chr4: 139,966,847-139,967,902 NOCT
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