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Items: 1 to 20 of 279

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5886478copy number variation1nstd209human GRCh38 chr1: 165,761,972-165,762,251 , GRCh37.p13 chr1: 165,731,209-165,731,488 TMCO1
    nsv5716839mobile element insertion1nstd211human GRCh38 chr1: 165,736,049-165,736,049 , GRCh37.p13 chr1: 165,705,286-165,705,286 TMCO1
    nsv5584199copy number variation1nstd207human GRCh38 chr1: 165,761,972-165,762,251 , GRCh37.p13 chr1: 165,731,209-165,731,488 TMCO1
    nsv5569207copy number variation1nstd207human GRCh38 chr1: 165,761,972-165,762,027 , GRCh37.p13 chr1: 165,731,209-165,731,264 TMCO1
    nsv5561047mobile element insertion1nstd206human GRCh38 chr1: 165,736,049-165,736,100 , GRCh37.p13 chr1: 165,705,286-165,705,337 TMCO1
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5371481translocation1nstd200human GRCh38 chr1: 165,769,259-165,769,259 , GRCh38 chr1: 164,958,581-164,958,581 , GRCh37.p13 chr1: 164,927,818-164,927,818 , GRCh37.p13 chr1: 165,738,496-165,738,496 TMCO1-AS1, TMCO1
    nsv5353968translocation1nstd200human GRCh38 chr1: 165,762,252-165,762,252 , GRCh38 chr1: 165,762,008-165,762,008 , GRCh37.p13 chr1: 165,731,489-165,731,489 , GRCh37.p13 chr1: 165,731,245-165,731,245 TMCO1
    nsv5344177translocation1nstd200human GRCh37 chr1: 165,731,489-165,731,489 , GRCh37 chr1: 165,731,245-165,731,245 , GRCh38.p12 chr1: 165,762,252-165,762,252 , GRCh38.p12 chr1: 165,762,008-165,762,008 TMCO1
    nsv5332462translocation1nstd200human GRCh37 chr1: 164,927,818-164,927,818 , GRCh37 chr1: 165,738,496-165,738,496 , GRCh38.p12 chr1: 164,958,581-164,958,581 , GRCh38.p12 chr1: 165,769,259-165,769,259 TMCO1-AS1, TMCO1
    nsv5322957translocation1nstd204human GRCh38.p13 chr1: 165,762,008-165,762,008 , GRCh38.p13 chr1: 165,762,252-165,762,252 , GRCh37.p13 chr1: 165,731,489-165,731,489 , GRCh37.p13 chr1: 165,731,245-165,731,245 TMCO1
    nsv5066580mobile element insertion1nstd203human GRCh38 chr1: 165,730,164-165,730,173 , GRCh37.p13 chr1: 165,699,401-165,699,410 TMCO1
    nsv5066106mobile element insertion1nstd203human GRCh38 chr1: 165,730,166-165,730,173 , GRCh37.p13 chr1: 165,699,403-165,699,410 TMCO1
    nsv5061702mobile element insertion1nstd203human GRCh38 chr1: 165,730,153-165,730,173 , GRCh37.p13 chr1: 165,699,390-165,699,410 TMCO1
    nsv5060409mobile element insertion1nstd203human GRCh38 chr1: 165,730,162-165,730,173 , GRCh37.p13 chr1: 165,699,399-165,699,410 TMCO1
    nsv5041452inversion1nstd200human GRCh38 chr1: 163,441,139-169,028,376 , GRCh37.p13 chr1: 163,410,929-168,997,614 , RPS17P6, 97 more genes
    nsv4897865copy number variation1nstd200human GRCh38 chr1: 165,769,258-165,771,239 , GRCh37.p13 chr1: 165,738,495-165,740,476 TMCO1-AS1, TMCO1
    nsv4897864copy number variation1nstd200human GRCh38 chr1: 165,728,316-165,730,625 , GRCh37.p13 chr1: 165,697,553-165,699,862 TMCO1
    nsv4784545copy number variation1nstd200human GRCh37 chr1: 165,738,495-165,740,476 , GRCh38.p12 chr1: 165,769,258-165,771,239 TMCO1, TMCO1-AS1
    nsv4784544copy number variation1nstd200human GRCh37 chr1: 165,720,069-165,720,664 , GRCh38.p12 chr1: 165,750,832-165,751,427 TMCO1
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