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Items: 1 to 20 of 242

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7140662insertion1nstd232human GRCh37.p13 chr15: 59,964,939-59,964,939 , GRCh38.p12 chr15: 59,672,740-59,672,740 BNIP2
    nsv7074787inversion1nstd229human GRCh38 chr15: 59,615,252-60,468,571 , GRCh37.p13 chr15: 59,907,451-60,760,770 BNIP2, ICE2, 14 more genes
    nsv7071327inversion1nstd229human GRCh38 chr15: 55,806,321-63,352,065 , GRCh37.p13 chr15: 56,098,519-63,644,264 LOC107984805, TPM1-AS, 120 more genes
    nsv7069841inversion1nstd229human GRCh38 chr15: 55,108,583-62,405,114 , GRCh37.p13 chr15: 55,400,781-62,697,313 LOC105370834, RPL21P14, 118 more genes
    nsv7059200inversion1nstd229human GRCh38 chr15: 59,449,988-59,734,427 , GRCh37.p13 chr15: 59,742,187-60,026,626 GTF2A2, PIGHP1, 6 more genes
    nsv6976334copy number variation1nstd229human GRCh38 chr15: 59,533,256-59,675,881 , GRCh37.p13 chr15: 59,825,455-59,968,080 BNIP2, GCNT3, 4 more genes
    nsv6975719copy number variation1nstd229human GRCh38 chr15: 59,681,182-59,727,356 , GRCh37.p13 chr15: 59,973,381-60,019,555 BNIP2
    nsv6973576copy number variation1nstd229human GRCh38 chr15: 59,666,220-59,666,398 , GRCh37.p13 chr15: 59,958,419-59,958,597 BNIP2
    nsv6973476copy number variation1nstd229human GRCh38 chr15: 59,672,324-59,674,753 , GRCh37.p13 chr15: 59,964,523-59,966,952 PIGHP1, BNIP2
    nsv6972336copy number variation1nstd229human GRCh38 chr15: 59,476,891-59,866,160 , GRCh37.p13 chr15: 59,769,090-60,158,359 GTF2A2, RPS3AP6, 7 more genes
    nsv6969701copy number variation1nstd229human GRCh38 chr15: 59,450,001-59,740,000 , GRCh37.p13 chr15: 59,742,200-60,032,199 GTF2A2, RPL21P114, 6 more genes
    nsv6963730copy number variation1nstd229human GRCh38 chr15: 59,636,442-59,681,432 , GRCh37.p13 chr15: 59,928,641-59,973,631 BNIP2, PIGHP1, 1 more genes
    nsv6962712copy number variation1nstd229human GRCh38 chr15: 59,661,809-59,662,238 , GRCh37.p13 chr15: 59,954,008-59,954,437 BNIP2
    nsv6959531copy number variation1nstd229human GRCh38 chr15: 59,683,725-59,685,239 , GRCh37.p13 chr15: 59,975,924-59,977,438 BNIP2
    nsv6637384copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,589,845-63,543,438 , GRCh38.p12 chr15: 48,297,648-63,251,239 LINC03065, FAM227B, 228 more genes
    nsv6623132copy number variation1nstd224human GRCh37 chr15: 59,951,997-59,992,758 , GRCh38.p12 chr15: 59,659,798-59,700,559 BNIP2, PIGHP1
    nsv6623131copy number variation1nstd224human GRCh37 chr15: 59,919,844-59,954,552 , GRCh38.p12 chr15: 59,627,645-59,662,353 GTF2A2, BNIP2
    nsv6623130copy number variation1nstd224human GRCh37 chr15: 59,894,617-59,997,696 , GRCh38.p12 chr15: 59,602,418-59,705,497 BNIP2, GCNT3, 2 more genes
    nsv6595054inversion1nstd223human GRCh38 chr15: 59,681,656-59,682,316 , GRCh37.p13 chr15: 59,973,855-59,974,515 BNIP2
    nsv6586822inversion1nstd223human GRCh38 chr15: 59,615,251-60,468,567 , GRCh37.p13 chr15: 59,907,450-60,760,766 PIGHP1, MESTP2, 14 more genes
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