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Items: 1 to 20 of 218

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1398546copy number variation1nstd102humanUncertain significance GRCh38 chr16: 70,855,202-71,067,341 , GRCh37 chr16: 70,889,105-71,101,244 HYDIN
    nsv1398222copy number variation1nstd102humanUncertain significance GRCh38 chr1: 20,810,811-20,829,210 , GRCh37 chr1: 21,137,304-21,155,703 EIF4G3
    nsv1398237copy number variation1nstd102humanUncertain significance GRCh37 chr6: 52,616,441-52,622,703 , GRCh38 chr6: 52,751,643-52,757,905 GSTA2
    nsv1398135copy number variation1nstd102humanUncertain significance GRCh38 chr1: 13,272,807-13,275,727 , GRCh37 chr1: 12,780,917-13,910,449 PRAMEF32P
    nsv4578690copy number variation1nstd102humanUncertain significance GRCh38 chr19: 1,508,507-1,510,399 , GRCh37 chr19: 1,508,506-1,510,398 ADAMTSL5
    nsv4578677copy number variation1nstd102humanUncertain significance GRCh38 chr1: 26,519,016-26,520,363 , GRCh37 chr1: 26,801,111-26,856,444 DPPA2P2
    nsv4578678copy number variation1nstd102humanUncertain significance GRCh38 chr20: 3,672,810-3,673,617 , GRCh37 chr20: 3,653,457-3,654,264 ADAM33
    nsv1398161copy number variation1nstd102humanUncertain significance GRCh37 chr1: 108,115,974-108,313,305 , GRCh38.p12 chr1: 107,573,352-107,770,683 VAV3
    nsv1398524copy number variation1nstd102humanUncertain significance GRCh37 chr9: 79,816,302-79,908,341 , GRCh38.p12 chr9: 77,201,386-77,293,425 VPS13A
    nsv1398549copy number variation1nstd102humanUncertain significance GRCh37 chr4: 104,035,661-104,119,449 , GRCh38.p12 chr4: 103,114,504-103,198,292 CENPE
    nsv1398398copy number variation1nstd102humanUncertain significance GRCh37 chr2: 170,009,392-170,072,852 , GRCh38.p12 chr2: 169,152,882-169,216,342 LRP2
    nsv1397959copy number variation1nstd102humanUncertain significance GRCh37 chr4: 169,325,195-169,379,102 , GRCh38.p12 chr4: 168,404,044-168,457,951 DDX60L
    nsv1397981copy number variation1nstd102humanUncertain significance GRCh37 chr5: 127,469,912-127,522,256 , GRCh38.p12 chr5: 128,134,220-128,186,564 SLC12A2
    nsv1398643copy number variation1nstd102humanUncertain significance GRCh37 chr8: 39,645,687-39,694,694 , GRCh38.p12 chr8: 39,788,168-39,837,175 , GRCh38.p12 chr8|NT_187577.1: 538,800-587,811 ADAM2
    nsv1398027copy number variation1nstd102humanUncertain significance GRCh37 chr15: 90,931,601-90,976,990 , GRCh38.p12 chr15: 90,388,369-90,433,758 IQGAP1
    nsv1398346copy number variation1nstd102humanUncertain significance GRCh37 chr1: 84,610,138-84,650,825 , GRCh38.p12 chr1: 84,144,455-84,185,142 PRKACB
    nsv1398514copy number variation1nstd102humanUncertain significance GRCh37 chr6: 167,412,952-167,447,412 , GRCh38.p12 chr6: 166,999,464-167,033,924 CEP43
    nsv1398518copy number variation1nstd102humanUncertain significance GRCh37 chr5: 64,817,329-64,847,428 , GRCh38.p12 chr5: 65,521,502-65,551,601 CENPK
    nsv1398134copy number variation1nstd102humanUncertain significance GRCh37 chr10: 27,326,892-27,356,151 , GRCh38.p12 chr10: 27,037,963-27,067,222 ANKRD26
    nsv1398602copy number variation1nstd102humanUncertain significance GRCh37 chr12: 76,763,038-76,780,400 , GRCh38.p12 chr12: 76,369,258-76,386,620 OSBPL8
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