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Items: 1 to 20 of 88

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5563339inversion1nstd206human GRCh38 chr5: 154,047,107-154,049,675 , GRCh37.p13 chr5: 153,426,667-153,429,235 MFAP3
    nsv5545531insertion1nstd206human GRCh38 chr5: 154,047,150-154,047,162 , GRCh37.p13 chr5: 153,426,710-153,426,722 MFAP3
    nsv5459047copy number variation1nstd206human GRCh38 chr5: 154,047,712-154,048,473 , GRCh37.p13 chr5: 153,427,272-153,428,033 MFAP3
    nsv5080438mobile element insertion1nstd203human GRCh38 chr5: 154,047,121-154,047,130 , GRCh37.p13 chr5: 153,426,681-153,426,690 MFAP3
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 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
    nsv4939315copy number variation1nstd200human GRCh38 chr5: 154,054,272-154,059,905 , GRCh37.p13 chr5: 153,433,832-153,439,465 MFAP3
    nsv4939314copy number variation1nstd200human GRCh38 chr5: 154,047,712-154,048,473 , GRCh37.p13 chr5: 153,427,272-153,428,033 MFAP3
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4131360copy number variation1nstd166human GRCh37.p13 chr5: 153,427,272-153,428,033 , GRCh38.p12 chr5: 154,047,712-154,048,473 MFAP3
    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
    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
    nsv3912593copy number variation1nstd102humanUncertain significance NCBI36 chr5: 332,389-180,837,866 , GRCh37.p13 chr5: 279,389-180,905,260 , GRCh38.p12 chr5: 279,274-181,478,259 LOC105378993, LOC107986375, 2492 more genes
    nsv3889848copy number variation1nstd102humanPathogenic GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719 MEGF10, LOC100128407, 2080 more genes
    nsv3886374copy number variation1nstd102humanPathogenic GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028 LOC105374618, HARS1, 2499 more genes
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