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Items: 1 to 20 of 482

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097229copy number variation1nstd102humanUncertain significance GRCh37 chr4: 126,237,567-126,337,797 , GRCh38.p12 chr4: 125,316,412-125,416,642 FAT4
    nsv7096979copy number variation1nstd102humanUncertain significance GRCh37 chr4: 126,237,567-126,412,923 , GRCh38.p12 chr4: 125,316,412-125,491,768 FAT4
    nsv7052737inversion1nstd229human GRCh38 chr4: 124,487,719-129,666,522 , GRCh37.p13 chr4: 125,408,874-130,587,677 H3P15, ANKRD50, 36 more genes
    nsv7046094inversion1nstd229human GRCh38 chr4: 125,385,516-125,385,574 , GRCh37.p13 chr4: 126,306,671-126,306,729 FAT4
    nsv6755139copy number variation1nstd229human GRCh38 chr4: 125,403,583-125,403,605 , GRCh37.p13 chr4: 126,324,738-126,324,760 FAT4
    nsv6755028copy number variation1nstd229human GRCh38 chr4: 125,415,001-125,424,700 , GRCh37.p13 chr4: 126,336,156-126,345,855 FAT4
    nsv6754208copy number variation1nstd229human GRCh38 chr4: 125,435,981-125,441,774 , GRCh37.p13 chr4: 126,357,136-126,362,929 FAT4
    nsv6753628copy number variation1nstd229human GRCh38 chr4: 125,368,842-125,386,496 , GRCh37.p13 chr4: 126,289,997-126,307,651 FAT4
    nsv6752962copy number variation1nstd229human GRCh38 chr4: 125,485,071-125,486,910 , GRCh37.p13 chr4: 126,406,226-126,408,065 FAT4
    nsv6752305copy number variation1nstd229human GRCh38 chr4: 125,334,371-125,356,873 , GRCh37.p13 chr4: 126,255,526-126,278,028 FAT4
    nsv6751256copy number variation1nstd229human GRCh38 chr4: 125,423,001-125,427,100 , GRCh37.p13 chr4: 126,344,156-126,348,255 FAT4
    nsv6750894copy number variation1nstd229human GRCh38 chr4: 125,293,117-125,564,359 , GRCh37.p13 chr4: 126,214,272-126,485,514 FAT4, MIR2054
    nsv6747258copy number variation1nstd229human GRCh38 chr4: 125,327,539-125,330,838 , GRCh37.p13 chr4: 126,248,694-126,251,993 FAT4
    nsv6745017copy number variation1nstd229human GRCh38 chr4: 125,429,888-125,429,942 , GRCh37.p13 chr4: 126,351,043-126,351,097 FAT4
    nsv6744885copy number variation1nstd229human GRCh38 chr4: 125,372,284-125,393,063 , GRCh37.p13 chr4: 126,293,439-126,314,218 FAT4
    nsv6743804copy number variation1nstd229human GRCh38 chr4: 125,236,446-125,425,164 , GRCh37.p13 chr4: 126,157,601-126,346,319 FAT4
    nsv6742474copy number variation1nstd229human GRCh38 chr4: 125,359,722-125,360,574 , GRCh37.p13 chr4: 126,280,877-126,281,729 FAT4
    nsv6740063copy number variation1nstd229human GRCh38 chr4: 125,419,545-125,430,063 , GRCh37.p13 chr4: 126,340,700-126,351,218 FAT4
    nsv6739945copy number variation1nstd229human GRCh38 chr4: 125,429,880-125,429,939 , GRCh37.p13 chr4: 126,351,035-126,351,094 FAT4
    nsv6738450copy number variation1nstd229human GRCh38 chr4: 125,356,471-125,362,846 , GRCh37.p13 chr4: 126,277,626-126,284,001 FAT4
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