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Items: 1 to 20 of 374

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5959579copy number variation1nstd209human GRCh38 chr22: 45,942,923-45,942,980 , GRCh37.p13 chr22: 46,338,803-46,338,860 WNT7B
    nsv5953613copy number variation1nstd209human GRCh38 chr22: 45,953,134-45,953,225 , GRCh37.p13 chr22: 46,349,014-46,349,105 WNT7B
    nsv5953224copy number variation1nstd209human GRCh38 chr22: 45,967,454-45,967,504 , GRCh37.p13 chr22: 46,363,334-46,363,384 WNT7B
    nsv5951699copy number variation1nstd209human GRCh38 chr22: 45,929,375-45,929,494 , GRCh37.p13 chr22: 46,325,255-46,325,374 WNT7B
    nsv5669288insertion1nstd207human GRCh38 chr22: 45,929,977-45,929,977 , GRCh37.p13 chr22: 46,325,857-46,325,857 WNT7B
    nsv5668688insertion1nstd207human GRCh38 chr22: 45,929,678-45,929,678 , GRCh37.p13 chr22: 46,325,558-46,325,558 WNT7B
    nsv5596500copy number variation1nstd207human GRCh38 chr22: 45,942,923-45,942,980 , GRCh37.p13 chr22: 46,338,803-46,338,860 WNT7B
    nsv5591661copy number variation1nstd207human GRCh38 chr22: 45,953,134-45,953,253 , GRCh37.p13 chr22: 46,349,014-46,349,133 WNT7B
    nsv5590753copy number variation1nstd207human GRCh38 chr22: 45,967,454-45,967,504 , GRCh37.p13 chr22: 46,363,334-46,363,384 WNT7B
    nsv5588624copy number variation1nstd207human GRCh38 chr22: 45,929,375-45,929,494 , GRCh37.p13 chr22: 46,325,255-46,325,374 WNT7B
    nsv5586199copy number variation1nstd207human GRCh38 chr22: 45,925,050-45,925,111 , GRCh37.p13 chr22: 46,320,930-46,320,991 WNT7B
    nsv5558258sequence alteration1nstd206human GRCh38 chr22: 45,946,489-45,949,870 , GRCh37.p13 chr22: 46,342,369-46,345,750 WNT7B
    nsv5553476copy number variation1nstd206human GRCh38 chr22: 45,955,146-45,955,484 , GRCh37.p13 chr22: 46,351,026-46,351,364 WNT7B
    nsv5551210copy number variation1nstd206human GRCh38 chr22: 45,929,810-45,929,872 , GRCh37.p13 chr22: 46,325,690-46,325,752 WNT7B
    nsv5548463copy number variation1nstd206human GRCh38 chr22: 45,939,745-45,940,215 , GRCh37.p13 chr22: 46,335,625-46,336,095 WNT7B
    nsv5546143copy number variation1nstd206human GRCh38 chr22: 45,929,870-45,929,924 , GRCh37.p13 chr22: 46,325,750-46,325,804 WNT7B
    nsv5545722copy number variation1nstd206human GRCh38 chr22: 45,937,807-45,938,408 , GRCh37.p13 chr22: 46,333,687-46,334,288 WNT7B
    nsv5539389copy number variation1nstd206human GRCh38 chr22: 45,967,455-45,967,505 , GRCh37.p13 chr22: 46,363,335-46,363,385 WNT7B
    nsv5537492copy number variation1nstd206human GRCh38 chr22: 45,976,059-45,976,109 , GRCh37.p13 chr22: 46,371,939-46,371,989 WNT7B
    nsv5535716insertion1nstd206human GRCh38 chr22: 45,949,665-45,949,665 , GRCh37.p13 chr22: 46,345,545-46,345,545 WNT7B
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