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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148155copy number variation1nstd102humanPathogenic GRCh37 chr17: 72,718,277-74,142,256 , GRCh38.p12 chr17: 74,722,138-76,146,175 TRIM65, TEN1, 74 more genes
    nsv7098900copy number variation1nstd102humanUncertain significance GRCh37 chr17: 72,864,876-73,328,878 , GRCh38.p12 chr17: 74,868,753-75,332,797 CDR2L, OTOP2, 28 more genes
    nsv6994090copy number variation1nstd229human GRCh38 chr17: 75,053,032-75,108,705 , GRCh37.p13 chr17: 73,049,127-73,104,800 SLC16A5, TRIM80P, 2 more genes
    nsv6989264copy number variation1nstd229human GRCh38 chr17: 75,054,571-75,057,926 , GRCh37.p13 chr17: 73,050,666-73,054,021 KCTD2
    nsv6985535copy number variation1nstd229human GRCh38 chr17: 75,060,282-75,067,074 , GRCh37.p13 chr17: 73,056,377-73,063,169 KCTD2
    nsv6985463copy number variation1nstd229human GRCh38 chr17: 75,023,356-75,035,089 , GRCh37.p13 chr17: 73,019,451-73,031,184 TRR-TCG3-1, KCTD2, 3 more genes
    nsv6985303copy number variation1nstd229human GRCh38 chr17: 75,042,760-75,046,636 , GRCh37.p13 chr17: 73,038,855-73,042,731 KCTD2, ATP5PD
    nsv6984264copy number variation1nstd229human GRCh38 chr17: 74,239,313-78,611,254 , GRCh37.p13 chr17: 72,235,452-76,607,336 SNORD1C, PRCD, 178 more genes
    nsv6982661copy number variation1nstd229human GRCh38 chr17: 75,044,187-75,044,504 , GRCh37.p13 chr17: 73,040,282-73,040,599 KCTD2, ATP5PD
    nsv6978648copy number variation1nstd229human GRCh38 chr17: 75,065,092-75,065,671 , GRCh37.p13 chr17: 73,061,187-73,061,766 KCTD2
    nsv6624308copy number variation1nstd224human GRCh37 chr17: 72,877,346-73,127,348 , GRCh38.p12 chr17: 74,881,216-75,131,253 SLC16A5, KCTD2, 18 more genes
    nsv6593991inversion1nstd223human GRCh38 chr17: 75,057,073-75,058,542 , GRCh37.p13 chr17: 73,053,168-73,054,637 KCTD2
    nsv6583385inversion1nstd223human GRCh38 chr17: 75,035,831-75,036,248 , GRCh37.p13 chr17: 73,031,926-73,032,343 KCTD2
    nsv6580372inversion1nstd223human GRCh38 chr17: 72,236,607-79,483,477 , GRCh37.p13 chr17: 70,232,748-77,412,076 TNRC6C, PTMAP13, 217 more genes
    nsv6533160copy number variation1nstd223human GRCh38 chr17: 75,021,713-75,030,836 , GRCh37.p13 chr17: 73,017,808-73,026,931 MRPL58, KCTD2, 1 more genes
    nsv6529637copy number variation1nstd223human GRCh38 chr17: 75,065,092-75,065,668 , GRCh37.p13 chr17: 73,061,187-73,061,763 KCTD2
    nsv6525954copy number variation1nstd223human GRCh38 chr17: 75,046,301-75,048,100 , GRCh37.p13 chr17: 73,042,396-73,044,195 ATP5PD, KCTD2
    nsv6519372copy number variation1nstd223human GRCh38 chr17: 75,044,187-75,044,504 , GRCh37.p13 chr17: 73,040,282-73,040,599 KCTD2, ATP5PD
    nsv6515680copy number variation1nstd223human GRCh38 chr17: 75,035,605-75,037,074 , GRCh37.p13 chr17: 73,031,700-73,033,169 TRR-TCG3-1, KCTD2, 1 more genes
    nsv6314018copy number variation1nstd102humanUncertain significance GRCh37 chr17: 73,049,227-73,533,226 , GRCh38.p12 chr17: 75,053,132-75,537,145 MIF4GD-DT, TSEN54, 21 more genes
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