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Items: 1 to 20 of 243

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057108inversion1nstd229human GRCh38 chr4: 154,728,774-156,655,899 , GRCh37.p13 chr4: 155,649,926-157,577,051 RNU2-66P, LOC105377501, 38 more genes
    nsv7048230inversion1nstd229human GRCh38 chr4: 149,781,104-157,324,460 , GRCh37.p13 chr4: 150,702,256-158,245,612 LOC107986197, LINC02273, 119 more genes
    nsv6756229copy number variation1nstd229human GRCh38 chr4: 155,330,945-155,381,176 , GRCh37.p13 chr4: 156,252,097-156,302,328 YWHAEP4, MAP9-AS1, 1 more genes
    nsv6752961copy number variation1nstd229human GRCh38 chr4: 155,358,401-155,367,300 , GRCh37.p13 chr4: 156,279,553-156,288,452 MAP9, MAP9-AS1
    nsv6751123copy number variation1nstd229human GRCh38 chr4: 155,358,509-155,399,200 , GRCh37.p13 chr4: 156,279,661-156,320,352 LOC100420289, MAP9, 2 more genes
    nsv6744002copy number variation1nstd229human GRCh38 chr4: 155,270,144-155,371,502 , GRCh37.p13 chr4: 156,191,296-156,292,654 MAP9-AS1, MAP9, 1 more genes
    nsv6741441copy number variation1nstd229human GRCh38 chr4: 155,372,729-155,382,897 , GRCh37.p13 chr4: 156,293,881-156,304,049 MAP9, LOC100420289, 1 more genes
    nsv6740441copy number variation1nstd229human GRCh38 chr4: 155,337,901-155,347,300 , GRCh37.p13 chr4: 156,259,053-156,268,452 MAP9
    nsv6629189copy number variation2nstd224human GRCh37 chr4: 156,198,222-156,288,089 , GRCh38.p12 chr4: 155,277,070-155,366,937 MAP9, MAP9-AS1, 1 more genes
    nsv6555609inversion1nstd223human GRCh38 chr4: 155,354,532-155,356,093 , GRCh37.p13 chr4: 156,275,684-156,277,245 MAP9, MAP9-AS1
    nsv6392864copy number variation1nstd223human GRCh38 chr4: 155,365,258-155,365,950 , GRCh37.p13 chr4: 156,286,410-156,287,102 MAP9
    nsv6382175copy number variation1nstd223human GRCh38 chr4: 155,337,924-155,347,265 , GRCh37.p13 chr4: 156,259,076-156,268,417 MAP9
    nsv6134914copy number variation1nstd213human GRCh37 chr4: 156,190,000-156,650,001 , GRCh38.p12 chr4: 155,268,848-155,728,849 GUCY1A1, MAP9, 21 more genes
    nsv6134911copy number variation1nstd213human GRCh37 chr4: 147,270,000-190,610,001 , GRCh38.p12 chr4: 146,348,848-189,688,847 , AGA, 517 more genes
    nsv6134884copy number variation1nstd213human GRCh37 chr4: 109,230,000-161,720,001 , GRCh38.p12 chr4: 108,308,844-160,798,849 , ANK2, 616 more genes
    nsv6134731copy number variation1nstd213human GRCh37 chr4: 109,230,000-161,710,001 , GRCh38.p12 chr4: 108,308,844-160,788,849 , ANK2, 616 more genes
    nsv6112754copy number variation1nstd102humanPathogenic GRCh37 chr4: 131,303,317-168,722,402 , GRCh38.p12 chr4: 130,382,162-167,801,251 MIR3139, CLGN, 407 more genes
    nsv6062649insertion1nstd212human GRCh38 chr4: 155,349,264-155,349,264 , GRCh37.p13 chr4: 156,270,416-156,270,416 MAP9
    nsv5995515copy number variation1nstd212human GRCh38 chr4: 155,349,248-155,349,307 , GRCh37.p13 chr4: 156,270,400-156,270,459 MAP9
    nsv5995514copy number variation1nstd212human GRCh38 chr4: 155,343,460-155,409,898 , GRCh37.p13 chr4: 156,264,612-156,331,050 MAP9, LOC100420289, 2 more genes
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