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Items: 1 to 20 of 119

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5677765mobile element insertion1nstd211human GRCh38 chr5: 163,473,755-163,473,755 , GRCh37.p13 chr5: 162,900,761-162,900,761 HMMR
    nsv5396843mobile element insertion1nstd206human GRCh38 chr5: 163,473,755-163,473,806 , GRCh37.p13 chr5: 162,900,761-162,900,812 HMMR
    nsv5377753translocation1nstd200human GRCh38 chr5: 163,460,643-163,460,643 , GRCh38 chr4: 167,230,503-167,230,503 , GRCh37.p13 chr5: 162,887,649-162,887,649 , GRCh37.p13 chr4: 168,151,654-168,151,654 HMMR, SPOCK3
    nsv5377752translocation1nstd200human GRCh38 chr5: 163,460,641-163,460,641 , GRCh38 chr4: 167,229,783-167,229,783 , GRCh37.p13 chr4: 168,150,934-168,150,934 , GRCh37.p13 chr5: 162,887,647-162,887,647 HMMR, SPOCK3
    nsv5333236translocation1nstd200human GRCh37 chr5: 162,887,647-162,887,647 , GRCh37 chr4: 168,150,934-168,150,934 , GRCh38.p12 chr4: 167,229,783-167,229,783 , GRCh38.p12 chr5: 163,460,641-163,460,641 SPOCK3, HMMR
    nsv5301541copy number variation1nstd204human GRCh38.p13 chr5: 163,429,687-163,899,395 , GRCh37.p13 chr5: 162,856,693-163,326,401 CCNG1, HMMR-AS1, 8 more genes
    nsv5238056copy number variation1nstd204human GRCh38.p13 chr5: 163,435,672-163,459,185 , GRCh37.p13 chr5: 162,862,678-162,886,191 LOC105377700, NUDCD2, 2 more genes
    nsv5220639copy number variation1nstd204human GRCh38.p13 chr5: 163,430,401-163,899,400 , GRCh37.p13 chr5: 162,857,407-163,326,406 HMMR, CCNG1, 8 more genes
    nsv4939644copy number variation1nstd200human GRCh38 chr5: 163,471,075-163,471,775 , GRCh37.p13 chr5: 162,898,081-162,898,781 HMMR
    nsv4939643copy number variation1nstd200human GRCh38 chr5: 163,462,654-163,463,557 , GRCh37.p13 chr5: 162,889,660-162,890,563 HMMR
    nsv4939642copy number variation1nstd200human GRCh38 chr5: 163,459,076-163,459,175 , GRCh37.p13 chr5: 162,886,082-162,886,181 HMMR, NUDCD2
    nsv4815312copy number variation1nstd200human GRCh37 chr5: 162,900,904-162,901,011 , GRCh38.p12 chr5: 163,473,898-163,474,005 HMMR
    nsv4815311copy number variation1nstd200human GRCh37 chr5: 162,898,081-162,898,781 , GRCh38.p12 chr5: 163,471,075-163,471,775 HMMR
    nsv4815310copy number variation1nstd200human GRCh37 chr5: 162,889,660-162,890,563 , GRCh38.p12 chr5: 163,462,654-163,463,557 HMMR
    nsv4684271copy number variation1nstd102humanUncertain significance GRCh37 chr5: 161,880,996-162,958,461 , GRCh38.p12 chr5: 162,453,990-163,531,455 MRPL57P6, ARL2BPP5, 10 more genes
    nsv4674945copy number variation1nstd102humanPathogenic GRCh37 chr5: 156,347,980-169,959,880 , GRCh38.p12 chr5: 156,920,969-170,532,876 LINC02227, LINC01932, 146 more genes
    nsv4597863copy number variation1nstd183human GRCh37 chr5: 162,537,788-163,536,134 , GRCh38.p12 chr5: 163,110,782-164,109,128 LOC102724458, NUDCD2, 8 more genes
    nsv4590428copy number variation1nstd183human GRCh37 chr5: 162,910,061-162,911,009 , GRCh38.p12 chr5: 163,483,055-163,484,003 HMMR, HMMR-AS1
    nsv4590427copy number variation1nstd183human GRCh37 chr5: 162,890,707-162,891,060 , GRCh38.p12 chr5: 163,463,701-163,464,054 HMMR
    nsv4456207copy number variation1nstd102humanUncertain significance GRCh37 chr5: 162,636,748-163,072,415 , GRCh38.p12 chr5: 163,209,742-163,645,409 NUDCD2, HMMR-AS1, 4 more genes
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