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Items: 1 to 20 of 220

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5645417insertion1nstd207human GRCh38 chr15: 89,663,571-89,663,571 , GRCh37.p13 chr15: 90,206,802-90,206,802 PLIN1, KIF7
    nsv5586724copy number variation1nstd207human GRCh38 chr15: 89,663,551-89,663,630 , GRCh37.p13 chr15: 90,206,782-90,206,861 PLIN1, KIF7
    nsv5528844copy number variation1nstd206human GRCh38 chr15: 89,660,415-89,660,476 , GRCh37.p13 chr15: 90,203,646-90,203,707 KIF7
    nsv5524665copy number variation1nstd206human GRCh38 chr15: 89,658,821-89,659,007 , GRCh37.p13 chr15: 90,202,052-90,202,238 KIF7
    nsv5523328copy number variation1nstd206human GRCh38 chr15: 89,629,240-89,629,349 , GRCh37.p13 chr15: 90,172,471-90,172,580 KIF7
    nsv5514282copy number variation1nstd206human GRCh38 chr15: 89,630,835-89,630,893 , GRCh37.p13 chr15: 90,174,066-90,174,124 KIF7
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5311805copy number variation1nstd204human GRCh38.p13 chr15: 89,658,812-89,659,015 , GRCh37.p13 chr15: 90,202,043-90,202,246 KIF7
    nsv5009156copy number variation1nstd200human GRCh38 chr15: 89,658,821-89,659,007 , GRCh37.p13 chr15: 90,202,052-90,202,238 KIF7
    nsv5009155copy number variation1nstd200human GRCh38 chr15: 89,613,141-89,651,335 , GRCh37.p13 chr15: 90,156,372-90,194,566 KIF7, TICRR
    nsv5009154copy number variation1nstd200human GRCh38 chr15: 89,564,220-89,658,106 , GRCh37.p13 chr15: 90,107,451-90,201,337 TICRR, KIF7
    nsv4863950copy number variation1nstd200human GRCh37 chr15: 90,156,372-90,194,566 , GRCh38.p12 chr15: 89,613,141-89,651,335 KIF7, TICRR
    nsv4765623insertion1nstd199human GRCh37 chr15: 90,206,811-90,206,811 , GRCh38.p12 chr15: 89,663,580-89,663,580 PLIN1, KIF7
    nsv4729092copy number variation1nstd102humanPathogenic GRCh37 chr15: 86,962,053-102,531,392 , GRCh38.p12 chr15: 86,418,822-101,981,189 CHD2, MIR11181, 272 more genes
    nsv4679244copy number variation1nstd189human GRCh37.p13 chr15: 89,903,203-90,447,762 , GRCh38.p12 chr15: 89,359,972-89,904,530 , ANPEP, 26 more genes
    nsv4675805copy number variation1nstd102humanUncertain significance GRCh37 chr15: 90,111,672-90,671,886 , GRCh38.p12 chr15: 89,568,441-90,128,654 RNU6-132P, PEX11A, 23 more genes
    nsv4675149copy number variation1nstd102humanPathogenic GRCh37 chr15: 87,189,245-102,429,112 , GRCh38.p12 chr15: 86,646,014-101,888,909 TTLL13, LINC00052, 264 more genes
    nsv4538680insertion1nstd166human GRCh37.p13 chr15: 90,188,475-90,188,475 , GRCh38.p12 chr15: 89,645,244-89,645,244 KIF7
    nsv4377776copy number variation1nstd173human GRCh37 chr15: 86,980,083-93,499,239 , GRCh38.p12 chr15: 86,436,852-92,956,009 , RNU6-1111P, 136 more genes
    nsv4350274copy number variation1nstd102humanPathogenic GRCh37 chr15: 83,883,823-92,165,844 , GRCh38.p12 chr15: 83,215,071-91,622,614 AKAP13, LOC105370972, 184 more genes
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