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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5956966insertion1nstd209human GRCh38 chr3: 111,077,344-111,077,344 , GRCh37.p13 chr3: 110,796,191-110,796,191 NECTIN3
    nsv5905995copy number variation1nstd209human GRCh38 chr3: 111,091,464-111,091,522 , GRCh37.p13 chr3: 110,810,311-110,810,369 NECTIN3
    nsv5900582copy number variation1nstd209human GRCh38 chr3: 111,166,975-111,167,072 , GRCh37.p13 chr3: 110,885,822-110,885,919 NECTIN3
    nsv5898863copy number variation1nstd209human GRCh38 chr3: 111,073,931-111,077,585 , GRCh37.p13 chr3: 110,792,778-110,796,432 NECTIN3
    nsv5893028copy number variation1nstd209human GRCh38 chr3: 111,129,835-111,129,991 , GRCh37.p13 chr3: 110,848,682-110,848,838 NECTIN3
    nsv5834529copy number variation1nstd209human GRCh38 chr3: 111,131,105-111,132,404 , GRCh37.p13 chr3: 110,849,952-110,851,251 NECTIN3
    nsv5834516copy number variation1nstd209human GRCh38 chr3: 111,197,169-111,235,690 , GRCh37.p13 chr3: 110,916,016-110,954,537 NECTIN3
    nsv5834276copy number variation1nstd209human GRCh38 chr3: 111,097,620-111,106,670 , GRCh37.p13 chr3: 110,816,467-110,825,517 NECTIN3
    nsv5834275copy number variation2nstd209human GRCh38 chr3: 111,073,871-111,077,396 , GRCh37.p13 chr3: 110,792,718-110,796,243 NECTIN3
    nsv5834274copy number variation2nstd209human GRCh38 chr3: 111,071,352-111,072,649 , GRCh37.p13 chr3: 110,790,199-110,791,496 NECTIN3
    nsv5833939copy number variation1nstd209human GRCh38 chr3: 111,089,658-111,093,488 , GRCh37.p13 chr3: 110,808,505-110,812,335 NECTIN3
    nsv5721346mobile element insertion1nstd211human GRCh38 chr3: 111,164,151-111,164,151 , GRCh37.p13 chr3: 110,882,998-110,882,998 NECTIN3
    nsv5716138mobile element insertion1nstd211human GRCh38 chr3: 111,080,630-111,080,630 , GRCh37.p13 chr3: 110,799,477-110,799,477 NECTIN3
    nsv5685370mobile element insertion1nstd211human GRCh38 chr3: 111,195,581-111,195,581 , GRCh37.p13 chr3: 110,914,428-110,914,428 NECTIN3
    nsv5682863mobile element insertion1nstd211human GRCh38 chr3: 111,077,363-111,077,363 , GRCh37.p13 chr3: 110,796,210-110,796,210 NECTIN3
    nsv5679209mobile element insertion2nstd211human GRCh38 chr3: 111,100,753-111,100,753 , GRCh37.p13 chr3: 110,819,600-110,819,600 NECTIN3
    nsv5621911insertion1nstd207human GRCh38 chr3: 111,100,741-111,100,741 , GRCh37.p13 chr3: 110,819,588-110,819,588 NECTIN3
    nsv5575981copy number variation1nstd207human GRCh38 chr3: 111,073,931-111,077,585 , GRCh37.p13 chr3: 110,792,778-110,796,432 NECTIN3
    nsv5452403copy number variation1nstd206human GRCh38 chr3: 111,201,472-111,205,323 , GRCh37.p13 chr3: 110,920,319-110,924,170 NECTIN3
    nsv5450870copy number variation1nstd206human GRCh38 chr3: 111,145,003-111,146,404 , GRCh37.p13 chr3: 110,863,850-110,865,251 NECTIN3
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