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Items: 1 to 20 of 325

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146499insertion1nstd232human GRCh37.p13 chr4: 100,510,225-100,510,225 , GRCh38.p12 chr4: 99,589,068-99,589,068 MTTP
    nsv7144601insertion1nstd232human GRCh37.p13 chr4: 100,510,232-100,510,232 , GRCh38.p12 chr4: 99,589,075-99,589,075 MTTP
    nsv7143553insertion1nstd232human GRCh37.p13 chr4: 100,510,192-100,510,192 , GRCh38.p12 chr4: 99,589,035-99,589,035 MTTP
    nsv7097219copy number variation1nstd102humanPathogenic GRCh37 chr4: 100,522,557-100,534,157 , GRCh38.p12 chr4: 99,601,400-99,613,000 MTTP
    nsv7097218copy number variation1nstd102humanPathogenic GRCh37 chr4: 100,485,243-100,504,684 , GRCh38.p12 chr4: 99,564,086-99,583,527 MTTP, TRMT10A
    nsv7096484copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 100,518,204-100,522,891 , GRCh38.p12 chr4: 99,597,047-99,601,734 MTTP
    nsv7096483copy number variation1nstd102humanPathogenic GRCh37 chr4: 100,470,245-100,544,005 , GRCh38.p12 chr4: 99,549,088-99,622,848 TRMT10A, MTTP
    nsv7096482copy number variation1nstd102humanPathogenic GRCh37 chr4: 100,239,320-100,528,137 , GRCh38.p12 chr4: 99,318,163-99,606,980 ADH1B, ADH1C, 5 more genes
    nsv7054609inversion1nstd229human GRCh38 chr4: 95,257,712-104,152,159 , GRCh37.p13 chr4: 96,178,863-105,073,316 SLC39A8, PABPC1P7, 96 more genes
    nsv7052845inversion1nstd229human GRCh38 chr4: 97,450,222-102,053,198 , GRCh37.p13 chr4: 98,371,373-102,974,355 RNU6-462P, LOC105377345, 58 more genes
    nsv7052661inversion1nstd229human GRCh38 chr4: 96,912,053-103,991,076 , GRCh37.p13 chr4: 97,833,204-104,912,233 MIR1255A, LOC107986297, 86 more genes
    nsv7046928inversion1nstd229human GRCh38 chr4: 95,051,434-103,882,549 , GRCh37.p13 chr4: 95,972,585-104,803,706 PABPC1P7, RN7SL728P, 95 more genes
    nsv7044544inversion1nstd229human GRCh38 chr4: 98,964,941-108,185,877 , GRCh37.p13 chr4: 99,886,092-109,107,033 LOC102725220, TACR3, 117 more genes
    nsv6755344copy number variation1nstd229human GRCh38 chr4: 99,540,229-99,709,776 , GRCh37.p13 chr4: 100,461,386-100,630,933 MTTP, C4orf17, 2 more genes
    nsv6755253copy number variation1nstd229human GRCh38 chr4: 99,618,401-99,666,000 , GRCh37.p13 chr4: 100,539,558-100,587,157 MTTP, C4orf54
    nsv6749738copy number variation1nstd229human GRCh38 chr4: 99,601,385-99,601,471 , GRCh37.p13 chr4: 100,522,542-100,522,628 MTTP
    nsv6747979copy number variation1nstd229human GRCh38 chr4: 99,611,231-99,624,969 , GRCh37.p13 chr4: 100,532,388-100,546,126 MTTP
    nsv6747044copy number variation1nstd229human GRCh38 chr4: 99,547,102-99,608,229 , GRCh37.p13 chr4: 100,468,259-100,529,386 MTTP, TRMT10A
    nsv6742761copy number variation1nstd229human GRCh38 chr4: 99,601,402-99,613,004 , GRCh37.p13 chr4: 100,522,559-100,534,161 MTTP
    nsv6568377inversion1nstd223human GRCh38 chr4: 99,562,177-99,562,542 , GRCh37.p13 chr4: 100,483,334-100,483,699 MTTP, TRMT10A
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