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Items: 1 to 20 of 110

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137085copy number variation1nstd102humanPathogenic GRCh37 chr5: 127,800,418-134,002,686 , GRCh38.p12 chr5: 128,464,725-134,666,996 CSF2, LOC402229, 99 more genes
    nsv7050047inversion1nstd229human GRCh38 chr5: 126,094,727-134,977,523 , GRCh37.p13 chr5: 125,430,420-134,313,213 RNU6-757P, SKP1, 145 more genes
    nsv7042985inversion1nstd229human GRCh38 chr5: 129,885,016-134,639,437 , GRCh37.p13 chr5: 129,220,709-133,975,127 HSPA8P4, LINC02999, 85 more genes
    nsv6795814copy number variation1nstd229human GRCh38 chr5: 132,864,618-132,865,162 , GRCh37.p13 chr5: 132,200,310-132,200,854 UQCRQ, GDF9
    nsv6787056copy number variation1nstd229human GRCh38 chr5: 126,804,198-136,494,917 , GRCh37.p13 chr5: 126,139,890-135,830,606 SLC22A4, LOC105379199, 158 more genes
    nsv6786929copy number variation1nstd229human GRCh38 chr5: 132,537,001-133,541,300 , GRCh37.p13 chr5: 131,872,693-132,876,991 ATP6V0E1P1, KIF3A, 27 more genes
    nsv6786470copy number variation1nstd229human GRCh38 chr5: 132,855,384-132,863,320 , GRCh37.p13 chr5: 132,191,076-132,199,012 GDF9
    nsv6780292copy number variation1nstd229human GRCh38 chr5: 132,866,422-132,943,701 , GRCh37.p13 chr5: 132,202,114-132,279,393 GDF9, EEF1A1P50, 3 more genes
    nsv6415295copy number variation1nstd223human GRCh38 chr5: 132,864,618-132,865,162 , GRCh37.p13 chr5: 132,200,310-132,200,854 UQCRQ, GDF9
    nsv6313595copy number variation1nstd102humanPathogenic GRCh37 chr5: 132,031,902-137,623,639 , GRCh38.p12 chr5: 132,696,210-138,287,950 TGFBI, RPS10P11, 110 more genes
    nsv6290726copy number variation1nstd102humanUncertain significance GRCh37 chr5: 132,181,132-132,605,222 , GRCh38.p12 chr5: 132,845,440-133,269,530 AFF4, ATP6V0E1P1, 13 more genes
    nsv6135646copy number variation1nstd213human GRCh37 chr5: 124,370,000-136,400,001 , GRCh38.p12 chr5: 125,034,307-137,064,312 ACTBP4, ALDH7A1, 181 more genes
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
    nsv6135113copy number variation1nstd213human GRCh37 chr5: 131,410,000-133,490,001 , GRCh38.p12 chr5: 132,074,307-134,154,310 CSF2, GDF9, 47 more genes
    nsv5893039copy number variation1nstd209human GRCh38 chr5: 132,864,618-132,865,161 , GRCh37.p13 chr5: 132,200,310-132,200,853 UQCRQ, GDF9
    nsv5632513insertion1nstd207human GRCh38 chr5: 132,864,618-132,864,618 , GRCh37.p13 chr5: 132,200,310-132,200,310 GDF9
    nsv5471660copy number variation1nstd206human GRCh38 chr5: 132,860,247-132,915,198 , GRCh37.p13 chr5: 132,195,939-132,250,890 GDF9, UQCRQ, 2 more genes
    nsv5461304copy number variation1nstd206human GRCh38 chr5: 132,864,618-132,865,164 , GRCh37.p13 chr5: 132,200,310-132,200,856 GDF9, UQCRQ
    nsv5362511translocation1nstd200human GRCh38 chr5: 132,864,618-132,864,618 , GRCh38 chr5: 132,865,164-132,865,164 , GRCh37.p13 chr5: 132,200,310-132,200,310 , GRCh37.p13 chr5: 132,200,856-132,200,856 UQCRQ, GDF9
    nsv5319150copy number variation1nstd204human GRCh38.p13 chr5: 132,864,616-132,865,165 , GRCh37.p13 chr5: 132,200,308-132,200,857 GDF9, UQCRQ
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