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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097139copy number variation1nstd102humanUncertain significance GRCh37 chr5: 33,944,753-39,364,566 , GRCh38.p12 chr5: 33,944,648-39,364,464 RNU7-75P, UGT3A1, 77 more genes
    nsv7051344inversion1nstd229human GRCh38 chr5: 36,271,641-38,407,431 , GRCh37.p13 chr5: 36,271,743-38,407,533 OFD1P17, NIPBL-DT, 29 more genes
    nsv7046165inversion1nstd229human GRCh38 chr5: 36,256,892-38,407,123 , GRCh37.p13 chr5: 36,256,994-38,407,225 NIPBL-DT, LINC02117, 29 more genes
    nsv7044509inversion1nstd229human GRCh38 chr5: 36,271,640-38,419,066 , GRCh37.p13 chr5: 36,271,742-38,419,168 WDR70, LINC02119, 29 more genes
    nsv6777854copy number variation1nstd229human GRCh38 chr5: 37,844,572-37,844,947 , GRCh37.p13 chr5: 37,844,674-37,845,049 GDNF-AS1
    nsv6771580copy number variation1nstd229human GRCh38 chr5: 37,217,581-37,839,425 , GRCh37.p13 chr5: 37,217,683-37,839,527 CPLANE1, WDR70, 9 more genes
    nsv6769429copy number variation1nstd229human GRCh38 chr5: 35,077,787-40,637,192 , GRCh37.p13 chr5: 35,077,889-40,637,294 LINC02110, LOC105374735, 68 more genes
    nsv6764862copy number variation1nstd229human GRCh38 chr5: 37,842,333-37,842,700 , GRCh37.p13 chr5: 37,842,435-37,842,802 GDNF-AS1
    nsv6764301copy number variation1nstd229human GRCh38 chr5: 37,395,324-40,706,253 , GRCh37.p13 chr5: 37,395,426-40,706,355 DAB2, LOC107986414, 39 more genes
    nsv6762559copy number variation1nstd229human GRCh38 chr5: 37,869,510-37,869,662 , GRCh37.p13 chr5: 37,869,612-37,869,764 GDNF-AS1
    nsv6762039copy number variation1nstd229human GRCh38 chr5: 37,751,739-37,947,795 , GRCh37.p13 chr5: 37,751,841-37,947,897 LINC02110, GDNF, 3 more genes
    nsv6760505copy number variation1nstd229human GRCh38 chr5: 37,853,613-37,853,650 , GRCh37.p13 chr5: 37,853,715-37,853,752 GDNF-AS1
    nsv6759067copy number variation1nstd229human GRCh38 chr5: 37,875,257-37,877,905 , GRCh37.p13 chr5: 37,875,359-37,878,007 GDNF-AS1
    nsv6636973copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,348,753-46,389,339 , GRCh38.p12 chr5: 29,348,646-46,389,237 SUB1, LOC105374740, 210 more genes
    nsv6391824copy number variation1nstd223human GRCh38 chr5: 37,603,316-38,357,867 , GRCh37.p13 chr5: 37,603,418-38,357,969 LINC02107, RNU6-1190P, 11 more genes
    nsv6391812copy number variation1nstd223human GRCh38 chr5: 37,875,252-37,877,901 , GRCh37.p13 chr5: 37,875,354-37,878,003 GDNF-AS1
    nsv6387815copy number variation1nstd223human GRCh38 chr5: 37,874,789-37,875,878 , GRCh37.p13 chr5: 37,874,891-37,875,980 GDNF-AS1
    nsv6375735copy number variation1nstd223human GRCh38 chr5: 37,751,739-37,947,791 , GRCh37.p13 chr5: 37,751,841-37,947,893 WDR70, LINC02117, 3 more genes
    nsv6315368copy number variation1nstd102humanPathogenic GRCh37 chr5: 36,053,583-46,389,339 , GRCh38.p12 chr5: 36,053,481-46,389,237 C7, RIMOC1, 128 more genes
    nsv6313864copy number variation1nstd102humanPathogenic GRCh37 chr5: 26,382,110-46,389,339 , GRCh38.p12 chr5: 26,382,001-46,389,237 LOC107986346, RNU6-760P, 227 more genes
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