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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143185insertion1nstd232human GRCh37.p13 chr7: 16,818,741-16,818,741 , GRCh38.p12 chr7: 16,779,116-16,779,116 TSPAN13
    nsv7097614copy number variation1nstd102humanUncertain significance GRCh37 chr7: 16,131,320-17,382,688 , GRCh38.p12 chr7: 16,091,695-17,343,064 BRWD1P3, ANKMY2, 19 more genes
    nsv7038576inversion1nstd229human GRCh38 chr7: 16,300,700-17,558,371 , GRCh37.p13 chr7: 16,340,325-17,597,995 LOC317727, LOC105375170, 21 more genes
    nsv6814842copy number variation1nstd229human GRCh38 chr7: 16,757,501-16,761,600 , GRCh37.p13 chr7: 16,797,126-16,801,225 TSPAN13
    nsv6814555copy number variation1nstd229human GRCh38 chr7: 16,769,801-16,804,000 , GRCh37.p13 chr7: 16,809,426-16,843,624 TSPAN13, AGR2
    nsv6813813copy number variation1nstd229human GRCh38 chr7: 16,700,023-16,752,925 , GRCh37.p13 chr7: 16,739,648-16,792,550 BZW2, TSPAN13
    nsv6810871copy number variation1nstd229human GRCh38 chr7: 16,504,503-17,165,581 , GRCh37.p13 chr7: 16,544,128-17,205,205 LRRC72, LOC105375169, 13 more genes
    nsv6808015copy number variation1nstd229human GRCh38 chr7: 16,765,163-16,766,993 , GRCh37.p13 chr7: 16,804,788-16,806,618 TSPAN13
    nsv6806859copy number variation1nstd229human GRCh38 chr7: 16,755,101-16,762,300 , GRCh37.p13 chr7: 16,794,726-16,801,925 TSPAN13
    nsv6804695copy number variation1nstd229human GRCh38 chr7: 16,756,142-16,759,709 , GRCh37.p13 chr7: 16,795,767-16,799,334 TSPAN13
    nsv6801340copy number variation1nstd229human GRCh38 chr7: 16,755,040-16,760,876 , GRCh37.p13 chr7: 16,794,665-16,800,501 TSPAN13
    nsv6799404copy number variation1nstd229human GRCh38 chr7: 16,359,233-17,380,982 , GRCh37.p13 chr7: 16,398,858-17,420,606 LOC101927609, SOSTDC1, 19 more genes
    nsv6798300copy number variation1nstd229human GRCh38 chr7: 16,755,811-16,760,258 , GRCh37.p13 chr7: 16,795,436-16,799,883 TSPAN13
    nsv6637135copy number variation1nstd102humanUncertain significance GRCh37 chr7: 15,639,869-16,963,424 , GRCh38.p12 chr7: 15,600,244-16,923,800 LOC105375166, LOC105375169, 20 more genes
    nsv6634397copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-19,485,604 , GRCh38.p12 chr7: 43,360-19,445,981 DNAAF5, FSCN1, 277 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6631678copy number variation1nstd224human GRCh37 chr7: 16,823,169-16,886,964 , GRCh38.p12 chr7: 16,783,544-16,847,340 TSPAN13, AGR2
    nsv6631613copy number variation1nstd224human GRCh37 chr7: 16,605,357-16,847,745 , GRCh38.p12 chr7: 16,565,732-16,808,121 AGR2, TSPAN13, 5 more genes
    nsv6631612copy number variation1nstd224human GRCh37 chr7: 16,500,142-17,040,226 , GRCh38.p12 chr7: 16,460,517-17,000,602 RAD17P1, LOC105375169, 12 more genes
    nsv6606975copy number variation1nstd223human GRCh38 chr7: 16,751,101-16,756,700 , GRCh37.p13 chr7: 16,790,726-16,796,325 TSPAN13
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