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Items: 1 to 20 of 84

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5966617insertion1nstd209human GRCh38 chr5: 154,452,793-154,452,793 , GRCh37.p13 chr5: 153,832,353-153,832,353 SAP30L
    nsv5685440mobile element insertion1nstd211human GRCh38 chr5: 154,457,432-154,457,432 , GRCh37.p13 chr5: 153,836,992-153,836,992 SAP30L
    nsv5469224copy number variation1nstd206human GRCh38 chr5: 154,452,711-154,452,815 , GRCh37.p13 chr5: 153,832,271-153,832,375 SAP30L
    nsv5394230mobile element insertion1nstd206human GRCh38 chr5: 154,457,432-154,457,483 , GRCh37.p13 chr5: 153,836,992-153,837,043 SAP30L
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv4949098copy number variation1nstd200human GRCh38 chr5: 154,399,687-154,546,399 , GRCh37.p13 chr5: 153,779,247-153,925,959 LOC100271907, LOC100128833, 4 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
    nsv4824338copy number variation1nstd200human GRCh37 chr5: 153,779,247-153,925,959 , GRCh38.p12 chr5: 154,399,687-154,546,399 SAP30L-AS1, HAND1, 4 more genes
    nsv4592591copy number variation1nstd183human GRCh37 chr5: 153,595,093-153,829,658 , GRCh38.p12 chr5: 154,215,533-154,450,098 GALNT10, SAP30L, 5 more genes
    nsv4455082copy number variation1nstd102humanUncertain significance GRCh37 chr5: 153,785,664-156,189,369 , GRCh38.p12 chr5: 154,406,104-156,762,358 CNOT8, RPL6P32, 25 more genes
    nsv4122978copy number variation1nstd166human GRCh37.p13 chr5: 153,369,866-154,042,234 , GRCh38.p12 chr5: 153,990,306-154,662,674 MFAP3, CIR1P1, 12 more genes
    nsv4116880copy number variation1nstd166human GRCh37.p13 chr5: 153,832,271-153,832,375 , GRCh38.p12 chr5: 154,452,711-154,452,815 SAP30L
    nsv3964370copy number variation1nstd168human GRCh38 chr5: 154,417,164-154,446,760 , GRCh37.p13 chr5: 153,796,724-153,826,320 SAP30L, GALNT10, 1 more genes
    nsv3923414copy number variation1nstd102humanPathogenic GRCh37 chr5: 130,196,621-154,701,371 , NCBI36 chr5: 130,224,520-154,681,564 , GRCh38 chr5: 130,860,928-155,321,811 HNRNPA3P7, RNU6-456P, 514 more genes
    nsv3922783copy number variation1nstd102humanPathogenic GRCh38 chr5: 152,761,187-167,248,053 , NCBI36 chr5: 152,120,940-166,607,636 , GRCh37 chr5: 152,140,747-166,675,058 APOOP1, LOC102724458, 151 more genes
    nsv3921182copy number variation1nstd102humanPathogenic GRCh37 chr5: 149,094,155-180,699,152 , GRCh38 chr5: 149,714,592-181,272,151 , NCBI36 chr5: 149,074,348-180,631,758 RN7SKP148, TCOF1, 553 more genes
    nsv3915958copy number variation1nstd102humanPathogenic GRCh38 chr5: 152,443,869-166,104,392 , NCBI36 chr5: 151,803,623-165,463,975 , GRCh37 chr5: 151,823,430-165,531,397 C5orf52, FAM114A2, 147 more genes
    nsv3914878copy number variation1nstd102humanPathogenic NCBI36 chr5: 146,520,648-163,194,778 , GRCh37.p13 chr5: 146,540,455-163,262,200 , GRCh38.p12 chr5: 147,160,892-163,835,194 LOC105378231, RN7SKP232, 247 more genes
    nsv3912937copy number variation1nstd102humanPathogenic GRCh37 chr5: 105,955,289-155,551,397 , NCBI36 chr5: 105,983,188-155,483,975 , GRCh38 chr5: 106,619,588-156,124,387 LINC01023, CTB-99A3.1, 783 more genes
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