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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
    nsv6793282copy number variation1nstd229human GRCh38 chr5: 133,124,433-133,167,876 , GRCh37.p13 chr5: 132,460,125-132,503,568 LOC105379178
    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
    nsv6780762copy number variation1nstd229human GRCh38 chr5: 132,897,401-133,154,000 , GRCh37.p13 chr5: 132,233,093-132,489,692 HSPA4, EEF1A1P50, 6 more genes
    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
    nsv5197860mobile element insertion1nstd203human GRCh38 chr5: 133,109,800-133,109,800 , GRCh37.p13 chr5: 132,445,492-132,445,492 LOC105379178
    nsv5186363mobile element insertion1nstd203human GRCh38 chr5: 133,109,784-133,109,784 , GRCh37.p13 chr5: 132,445,476-132,445,476 LOC105379178
    nsv5181383mobile element insertion1nstd203human GRCh38 chr5: 133,109,794-133,109,794 , GRCh37.p13 chr5: 132,445,486-132,445,486 LOC105379178
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv5034346inversion1nstd200human GRCh38 chr5: 99,223,339-135,778,784 , GRCh37.p13 chr5: 98,559,043-135,114,473 , NUDT12, 438 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4872282inversion1nstd200human GRCh37 chr5: 98,106,197-132,803,784 , GRCh38.p12 chr5: 98,770,493-133,468,092 , LEAP2, 395 more genes
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