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Items: 1 to 20 of 835

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5962690insertion1nstd209human GRCh38 chr4: 183,133,026-183,133,026 , GRCh37.p13 chr4: 184,054,179-184,054,179 WWC2
    nsv5906167copy number variation1nstd209human GRCh38 chr4: 183,226,357-183,230,406 , GRCh37.p13 chr4: 184,147,510-184,151,559 WWC2
    nsv5899986copy number variation1nstd209human GRCh38 chr4: 183,275,214-183,275,345 , GRCh37.p13 chr4: 184,196,367-184,196,498 WWC2
    nsv5897944copy number variation1nstd209human GRCh38 chr4: 183,184,872-183,185,133 , GRCh37.p13 chr4: 184,106,025-184,106,286 WWC2
    nsv5888856copy number variation1nstd209human GRCh38 chr4: 183,164,315-183,164,402 , GRCh37.p13 chr4: 184,085,468-184,085,555 WWC2
    nsv5838800copy number variation2nstd209human GRCh38 chr4: 183,319,490-183,322,008 , GRCh37.p13 chr4: 184,240,643-184,243,161 WWC2, CLDN24, 1 more genes
    nsv5838799copy number variation1nstd209human GRCh38 chr4: 183,121,867-183,123,366 , GRCh37.p13 chr4: 184,043,020-184,044,519 WWC2
    nsv5838738copy number variation1nstd209human GRCh38 chr4: 183,115,367-183,116,366 , GRCh37.p13 chr4: 184,036,520-184,037,519 WWC2
    nsv5838484copy number variation1nstd209human GRCh38 chr4: 183,312,191-183,313,290 , GRCh37.p13 chr4: 184,233,344-184,234,443 WWC2
    nsv5838483copy number variation1nstd209human GRCh38 chr4: 183,225,838-183,230,439 , GRCh37.p13 chr4: 184,146,991-184,151,592 WWC2
    nsv5692522mobile element insertion1nstd211human GRCh38 chr4: 183,154,031-183,154,031 , GRCh37.p13 chr4: 184,075,184-184,075,184 WWC2
    nsv5682321mobile element insertion2nstd211human GRCh38 chr4: 183,175,827-183,175,827 , GRCh37.p13 chr4: 184,096,980-184,096,980 WWC2
    nsv5643048insertion1nstd207human GRCh38 chr4: 183,175,811-183,175,811 , GRCh37.p13 chr4: 184,096,964-184,096,964 WWC2
    nsv5630413insertion1nstd207human GRCh38 chr4: 183,247,620-183,247,620 , GRCh37.p13 chr4: 184,168,773-184,168,773 WWC2
    nsv5626455insertion1nstd207human GRCh38 chr4: 183,133,024-183,133,024 , GRCh37.p13 chr4: 184,054,177-184,054,177 WWC2
    nsv5583515copy number variation1nstd207human GRCh38 chr4: 183,278,484-183,279,393 , GRCh37.p13 chr4: 184,199,637-184,200,546 WWC2
    nsv5578082copy number variation1nstd207human GRCh38 chr4: 183,164,303-183,164,397 , GRCh37.p13 chr4: 184,085,456-184,085,550 WWC2
    nsv5574277copy number variation1nstd207human GRCh38 chr4: 183,276,637-183,277,397 , GRCh37.p13 chr4: 184,197,790-184,198,550 WWC2
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5541767insertion1nstd206human GRCh38 chr4: 183,317,828-183,317,865 , GRCh37.p13 chr4: 184,238,981-184,239,018 WWC2, CLDN22
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