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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099236copy number variation1nstd231human GRCh38.p12 chr1: 156,064,931-157,804,884 , GRCh37 chr1: 156,034,722-157,774,674 BGLAP, CRABP2, 58 more genes
    nsv7055468inversion1nstd229human GRCh38 chr1: 155,667,181-158,101,472 , GRCh37.p13 chr1: 155,636,972-158,071,262 FCRL4, CRABP2, 88 more genes
    nsv7041047inversion1nstd229human GRCh38 chr1: 154,596,558-159,585,927 , GRCh37.p13 chr1: 154,569,034-159,555,717 ADAR, SNORA80E, 204 more genes
    nsv7039558inversion1nstd229human GRCh38 chr1: 155,298,171-158,468,090 , GRCh37.p13 chr1: 155,267,962-158,437,880 FCRL4, SCARNA4, 121 more genes
    nsv6642991copy number variation1nstd229human GRCh38 chr1: 157,037,338-157,044,241 , GRCh37.p13 chr1: 157,007,130-157,014,033 ARHGEF11
    nsv6642990copy number variation1nstd229human GRCh38 chr1: 157,027,955-157,033,897 , GRCh37.p13 chr1: 156,997,747-157,003,689 ARHGEF11
    nsv6642781copy number variation1nstd229human GRCh38 chr1: 157,034,226-157,043,677 , GRCh37.p13 chr1: 157,004,018-157,013,469 ARHGEF11
    nsv6642779copy number variation1nstd229human GRCh38 chr1: 156,967,031-156,972,465 , GRCh37.p13 chr1: 156,936,823-156,942,257 ARHGEF11
    nsv6642656copy number variation1nstd229human GRCh38 chr1: 156,919,252-156,967,854 , GRCh37.p13 chr1: 156,889,044-156,937,646 LRRC71, ARHGEF11, 1 more genes
    nsv6642547copy number variation1nstd229human GRCh38 chr1: 157,012,726-157,274,163 , GRCh37.p13 chr1: 156,982,518-157,243,953 LOC105371456, ARHGEF11, 8 more genes
    nsv6549694inversion1nstd223human GRCh38 chr1: 155,298,173-158,468,085 , GRCh37.p13 chr1: 155,267,964-158,437,875 ASH1L, GPATCH4, 121 more genes
    nsv6548406inversion1nstd223human GRCh38 chr1: 157,016,528-157,017,724 , GRCh37.p13 chr1: 156,986,320-156,987,516 ARHGEF11
    nsv6331838copy number variation1nstd223human GRCh38 chr1: 157,037,337-157,044,240 , GRCh37.p13 chr1: 157,007,129-157,014,032 ARHGEF11
    nsv6330841copy number variation1nstd223human GRCh38 chr1: 157,027,955-157,033,901 , GRCh37.p13 chr1: 156,997,747-157,003,693 ARHGEF11
    nsv6329527copy number variation1nstd223human GRCh38 chr1: 155,481,601-157,146,700 , GRCh37.p13 chr1: 155,451,392-157,116,492 BGLAP, SSR2, 78 more genes
    nsv6326600copy number variation1nstd223human GRCh38 chr1: 156,919,252-156,967,851 , GRCh37.p13 chr1: 156,889,044-156,937,643 LRRC71, MIR765, 1 more genes
    nsv6319004copy number variation1nstd223human GRCh38 chr1: 156,967,197-156,967,990 , GRCh37.p13 chr1: 156,936,989-156,937,782 ARHGEF11
    nsv6318568copy number variation1nstd223human GRCh38 chr1: 156,986,977-156,987,625 , GRCh37.p13 chr1: 156,956,769-156,957,417 ARHGEF11
    nsv6316931copy number variation1nstd223human GRCh38 chr1: 157,017,574-157,019,902 , GRCh37.p13 chr1: 156,987,366-156,989,694 ARHGEF11
    nsv6290596copy number variation1nstd102humanUncertain significance GRCh37 chr1: 156,665,257-156,902,706 , GRCh38.p12 chr1: 156,695,465-156,932,914 ISG20L2, PEAR1, 10 more genes
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