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Items: 1 to 20 of 172

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5954790insertion1nstd209human GRCh38 chr5: 133,102,913-133,102,913 , GRCh37.p13 chr5: 132,438,605-132,438,605 HSPA4
    nsv5953158insertion1nstd209human GRCh38 chr5: 133,085,489-133,085,489 , GRCh37.p13 chr5: 132,421,181-132,421,181 HSPA4
    nsv5892598copy number variation1nstd209human GRCh38 chr5: 133,060,420-133,061,722 , GRCh37.p13 chr5: 132,396,112-132,397,414 HSPA4
    nsv5187569mobile element insertion1nstd203human GRCh38 chr5: 133,093,778-133,093,797 , GRCh37.p13 chr5: 132,429,470-132,429,489 HSPA4
    nsv5177732mobile element insertion1nstd203human GRCh38 chr5: 133,087,145-133,087,159 , GRCh37.p13 chr5: 132,422,837-132,422,851 HSPA4
    nsv5091636mobile element insertion1nstd203human GRCh38 chr5: 133,085,489-133,085,502 , GRCh37.p13 chr5: 132,421,181-132,421,194 HSPA4
    nsv5083268mobile element insertion1nstd203human GRCh38 chr5: 133,087,145-133,087,159 , GRCh37.p13 chr5: 132,422,837-132,422,851 HSPA4
    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
    nsv4945081copy number variation1nstd200human GRCh38 chr5: 133,046,242-133,053,409 , GRCh37.p13 chr5: 132,381,934-132,389,101 HSPA4
    nsv4938625copy number variation1nstd200human GRCh38 chr5: 133,073,026-133,073,117 , GRCh37.p13 chr5: 132,408,718-132,408,809 HSPA4
    nsv4938624copy number variation1nstd200human GRCh38 chr5: 133,072,635-133,072,781 , GRCh37.p13 chr5: 132,408,327-132,408,473 HSPA4
    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
    nsv4778423mobile element deletion1nstd200human GRCh37 chr5: 132,389,351-132,389,650 , GRCh38.p12 chr5: 133,053,659-133,053,958 HSPA4
    nsv4567662mobile element insertion1nstd166human GRCh37.p13 chr5: 132,438,226-132,438,226 , GRCh38.p12 chr5: 133,102,534-133,102,534 HSPA4
    nsv4482600mobile element insertion1nstd166human GRCh37.p13 chr5: 132,411,639-132,411,639 , GRCh38.p12 chr5: 133,075,947-133,075,947 HSPA4
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
    nsv4320566inversion1nstd166human GRCh37.p13 chr5: 114,283,102-148,759,757 , GRCh38.p12 chr5: 114,947,405-149,380,194 , ACTBP4, 606 more genes
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