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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112729copy number variation1nstd102humannot provided GRCh37 chr5: 116,419,511-120,022,321 , GRCh38.p12 chr5: 117,083,815-120,686,626 RN7SL174P, LINC02148, 35 more genes
    nsv5840726copy number variation1nstd209human GRCh38 chr5: 119,533,576-119,534,675 , GRCh37.p13 chr5: 118,869,271-118,870,370 HSD17B4
    nsv5693590mobile element insertion2nstd211human GRCh38 chr5: 119,458,843-119,458,843 , GRCh37.p13 chr5: 118,794,538-118,794,538 HSD17B4
    nsv5690295mobile element insertion1nstd211human GRCh38 chr5: 119,460,838-119,460,838 , GRCh37.p13 chr5: 118,796,533-118,796,533 HSD17B4
    nsv5674715mobile element insertion1nstd211human GRCh38 chr5: 119,473,296-119,473,296 , GRCh37.p13 chr5: 118,808,991-118,808,991 HSD17B4
    nsv5673504copy number variation1nstd102humanPathogenic GRCh37 chr5: 118,865,579-118,867,109 , GRCh38.p12 chr5: 119,529,884-119,531,414 HSD17B4
    nsv5638204insertion1nstd207human GRCh38 chr5: 119,456,502-119,456,502 , GRCh37.p13 chr5: 118,792,197-118,792,197 HSD17B4
    nsv5470607copy number variation1nstd206human GRCh38 chr5: 119,517,349-119,517,785 , GRCh37.p13 chr5: 118,853,044-118,853,480 HSD17B4
    nsv5470564copy number variation1nstd206human GRCh38 chr5: 119,503,951-119,504,156 , GRCh37.p13 chr5: 118,839,646-118,839,851 HSD17B4
    nsv5399385mobile element insertion1nstd206human GRCh38 chr5: 119,458,843-119,458,894 , GRCh37.p13 chr5: 118,794,538-118,794,589 HSD17B4
    nsv5368871translocation1nstd200human GRCh38 chr5: 119,492,988-119,492,988 , GRCh38 chr5: 119,490,428-119,490,428 , GRCh37.p13 chr5: 118,828,683-118,828,683 , GRCh37.p13 chr5: 118,826,123-118,826,123 HSD17B4
    nsv5368870translocation1nstd200human GRCh38 chr5: 119,490,415-119,490,415 , GRCh38 chr5: 119,493,272-119,493,272 , GRCh37.p13 chr5: 118,826,110-118,826,110 , GRCh37.p13 chr5: 118,828,967-118,828,967 HSD17B4
    nsv5211090mobile element deletion1nstd204human GRCh38.p13 chr5: 119,459,845-119,460,200 , GRCh37.p13 chr5: 118,795,540-118,795,895 HSD17B4
    nsv5099086mobile element insertion1nstd203human GRCh38 chr5: 119,492,497-119,492,513 , GRCh37.p13 chr5: 118,828,192-118,828,208 HSD17B4
    nsv5084709mobile element insertion1nstd203human GRCh38 chr5: 119,458,830-119,458,843 , GRCh37.p13 chr5: 118,794,525-118,794,538 HSD17B4
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv5034346inversion1nstd200human GRCh38 chr5: 99,223,339-135,778,784 , GRCh37.p13 chr5: 98,559,043-135,114,473 , NUDT12, 438 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4944979copy number variation1nstd200human GRCh38 chr5: 119,503,951-119,504,156 , GRCh37.p13 chr5: 118,839,646-118,839,851 HSD17B4
    nsv4932598copy number variation1nstd200human GRCh38 chr5: 119,532,126-119,535,121 , GRCh37.p13 chr5: 118,867,821-118,870,816 HSD17B4
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