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Items: 1 to 20 of 399

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5944572copy number variation1nstd209human GRCh38 chr17: 46,210,492-47,098,378 , GRCh37.p13 chr17: 44,287,858-45,175,744 , KANSL1, 26 more genes
    nsv5655264insertion1nstd207human GRCh38 chr17: 46,777,891-46,777,891 , GRCh37.p13 chr17: 44,855,257-44,855,257 WNT3, LRRC37A2
    nsv5589268copy number variation1nstd207human GRCh38 chr17: 46,811,121-46,811,286 , GRCh37.p13 chr17: 44,888,487-44,888,652 LRRC37A2, WNT3
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5391296copy number variation1nstd186human GRCh37 chr17: 44,888,488-44,888,655 , GRCh38.p12 chr17: 46,811,122-46,811,289 , GRCh38.p12 chr17|NT_187663.1: 1,330,540-1,330,707 LRRC37A2, WNT3
    nsv5358902translocation1nstd200human GRCh38 chr17: 46,791,241-46,791,241 , GRCh38 chr17: 46,796,883-46,796,883 , GRCh37.p13 chr17: 44,868,607-44,868,607 , GRCh37.p13 chr17: 44,874,249-44,874,249 LRRC37A2, WNT3
    nsv5336472translocation1nstd200human GRCh37 chr17: 44,868,607-44,868,607 , GRCh37 chr17: 44,874,249-44,874,249 , GRCh38.p12 chr17: 46,791,241-46,791,241 , GRCh38.p12 chr17|NT_187663.1: 1,316,303-1,316,303 , GRCh38.p12 chr17|NT_167251.2: 1,777,133-1,777,133 , GRCh38.p12 chr17|NT_167251.2: 1,782,776-1,782,776 , GRCh38.p12 chr17: 46,796,883-46,796,883 , GRCh38.p12 chr17|NT_187663.1: 1,310,658-1,310,658 WNT3, LRRC37A2
    nsv5297500copy number variation1nstd204human GRCh38.p13 chr17: 46,811,101-46,811,300 , GRCh37.p13 chr17: 44,888,467-44,888,666 WNT3, LRRC37A2
    nsv4867162copy number variation1nstd200human GRCh37 chr17: 44,888,488-44,888,655 , GRCh38.p12 chr17: 46,811,122-46,811,289 , GRCh38.p12 chr17|NT_187663.1: 1,330,540-1,330,707 WNT3, LRRC37A2
    nsv4636250copy number variation1nstd186human GRCh37 chr17: 44,888,182-44,888,655 , GRCh38.p12 chr17|NT_167251.2: 1,796,709-1,797,015 , GRCh38.p12 chr17: 46,810,816-46,811,289 , GRCh38.p12 chr17|NT_187663.1: 1,330,234-1,330,707 WNT3, LRRC37A2
    nsv4627843copy number variation1nstd183human GRCh37 chr17: 44,848,454-44,849,701 , GRCh38.p12 chr17|NT_187663.1: 1,290,500-1,291,742 , GRCh38.p12 chr17: 46,771,088-46,772,335 , GRCh38.p12 chr17|NT_167251.2: 1,756,967-1,758,209 WNT3, LRRC37A2
    nsv4626525copy number variation1nstd183human GRCh37 chr17: 44,281,452-45,168,501 , GRCh38.p12 chr17: 46,204,086-47,091,135 , GRCh38.p12 chr17|NT_187663.1: 906,188-1,423,190 , NSF, 26 more genes
    nsv4557422mobile element insertion1nstd166human GRCh37.p13 chr17: 44,863,353-44,863,353 , GRCh38.p12 chr17|NT_187663.1: 1,305,398-1,305,398 , GRCh38.p12 chr17: 46,785,987-46,785,987 , GRCh38.p12 chr17|NT_167251.2: 1,771,873-1,771,873 LRRC37A2, WNT3
    nsv4531650copy number variation1nstd166human GRCh37.p13 chr17: 44,856,857-44,857,183 , GRCh38.p12 chr17: 46,779,491-46,779,817 , GRCh38.p12 chr17|NT_187663.1: 1,298,906-1,299,231 , GRCh38.p12 chr17|NT_167251.2: 1,765,377-1,765,703 LRRC37A2, WNT3
    nsv4514197mobile element insertion1nstd166human GRCh37.p13 chr17: 44,859,687-44,859,687 , GRCh38.p12 chr17: 46,782,321-46,782,321 , GRCh38.p12 chr17|NT_187663.1: 1,301,734-1,301,734 , GRCh38.p12 chr17|NT_167251.2: 1,768,207-1,768,207 WNT3, LRRC37A2
    nsv4430447copy number variation1nstd174human GRCh37 chr17: 44,848,438-44,849,701 , GRCh38.p12 chr17|NT_167251.2: 1,756,951-1,758,209 , GRCh38.p12 chr17: 46,771,072-46,772,335 , GRCh38.p12 chr17|NT_187663.1: 1,290,484-1,291,742 LRRC37A2, WNT3
    nsv4420591copy number variation1nstd174human GRCh37 chr17: 44,170,127-45,168,501 , GRCh38.p12 chr17: 46,092,761-47,091,135 , GRCh38.p12 chr17|NT_187663.1: 794,867-1,423,190 , ARL17A, 28 more genes
    nsv4413784copy number variation1nstd174human GRCh37 chr17: 44,888,482-44,888,672 , GRCh38.p12 chr17: 46,811,116-46,811,306 , GRCh38.p12 chr17|NT_187663.1: 1,330,534-1,330,724 LRRC37A2, WNT3
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4259327copy number variation1nstd166human GRCh37.p13 chr17: 44,845,299-44,845,401 , GRCh38.p12 chr17|NT_167251.2: 1,753,812-1,753,914 , GRCh38.p12 chr17: 46,767,933-46,768,035 , GRCh38.p12 chr17|NT_187663.1: 1,287,346-1,287,448 LRRC37A2, WNT3
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