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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7068226inversion1nstd229human GRCh38 chr17: 44,779,759-44,819,356 , GRCh37.p13 chr17: 42,857,127-42,896,724 ADAM11, GJC1
    nsv6996752copy number variation1nstd229human GRCh38 chr17: 44,583,598-44,869,402 , GRCh37.p13 chr17: 42,660,966-42,946,770 GJC1, CCDC43, 11 more genes
    nsv6983313copy number variation1nstd229human GRCh38 chr17: 44,722,067-44,774,913 , GRCh37.p13 chr17: 42,799,435-42,852,281 DBF4B, ADAM11, 1 more genes
    nsv6982861copy number variation1nstd229human GRCh38 chr17: 38,291,672-47,498,259 , GRCh37.p13 chr17: 36,510,266-45,575,625 KRT20, PLEKHH3, 442 more genes
    nsv6979407copy number variation1nstd229human GRCh38 chr17: 44,778,684-44,778,739 , GRCh37.p13 chr17: 42,856,052-42,856,107 ADAM11
    nsv6577256inversion1nstd223human GRCh38 chr17: 44,772,858-44,808,462 , GRCh37.p13 chr17: 42,850,226-42,885,830 GJC1, ADAM11
    nsv6189188copy number variation1nstd214human GRCh38 chr17: 44,778,683-44,778,738 , GRCh37.p13 chr17: 42,856,051-42,856,106 ADAM11
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5514983copy number variation1nstd206human GRCh38 chr17: 44,778,684-44,778,739 , GRCh37.p13 chr17: 42,856,052-42,856,107 ADAM11
    nsv5322509copy number variation1nstd204human GRCh37.p13 chr17: 42,834,773-42,880,824 , GRCh38.p13 chr17: 44,757,405-44,803,456 GJC1, ADAM11
    nsv5289464copy number variation1nstd204human GRCh38.p13 chr17: 44,757,301-44,803,500 , GRCh37.p13 chr17: 42,834,669-42,880,868 GJC1, ADAM11
    nsv5284866copy number variation1nstd204human GRCh38.p13 chr17: 44,757,102-44,777,215 , GRCh37.p13 chr17: 42,834,470-42,854,583 ADAM11
    nsv5156529mobile element insertion1nstd203human GRCh38 chr17: 44,763,874-44,763,888 , GRCh37.p13 chr17: 42,841,242-42,841,256 ADAM11
    nsv5148612mobile element insertion1nstd203human GRCh38 chr17: 44,778,688-44,778,698 , GRCh37.p13 chr17: 42,856,056-42,856,066 ADAM11
    nsv5013744copy number variation1nstd200human GRCh38 chr17: 44,752,408-44,771,054 , GRCh37.p13 chr17: 42,829,776-42,848,422 DBF4B, ADAM11
    nsv5013743copy number variation1nstd200human GRCh38 chr17: 44,722,067-44,774,913 , GRCh37.p13 chr17: 42,799,435-42,852,281 ADAM11, DBF4B, 1 more genes
    nsv4864676copy number variation1nstd200human GRCh37 chr17: 42,829,776-42,848,422 , GRCh38.p12 chr17: 44,752,408-44,771,054 ADAM11, DBF4B
    nsv4632617copy number variation1nstd183human GRCh37 chr17: 42,849,798-42,849,892 , GRCh38.p12 chr17: 44,772,430-44,772,524 ADAM11
    nsv4631146copy number variation1nstd183human GRCh37 chr17: 42,847,358-42,847,412 , GRCh38.p12 chr17: 44,769,990-44,770,044 ADAM11
    nsv4628164copy number variation1nstd183human GRCh37 chr17: 42,836,591-42,836,635 , GRCh38.p12 chr17: 44,759,223-44,759,267 ADAM11
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