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Items: 1 to 20 of 537

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146915insertion1nstd232human GRCh37.p13 chr4: 70,874,791-70,874,791 , GRCh38.p12 chr4: 70,009,074-70,009,074 , GRCh38.p12 chr4|NW_013171801.1: 49,210-49,210 0
    nsv6629776copy number variation1nstd224human GRCh37 chr4: 70,620,387-71,081,038 , GRCh38.p12 chr4: 69,754,669-70,215,321 , GRCh38.p12 chr4|NW_013171801.1: 1-236,512 CSN2, HTN1, 12 more genes
    nsv6314274complex chromosomal rearrangement2nstd102humanUncertain significance GRCh38.p12 chr4: 51,979,994-51,979,994 , GRCh38.p12 chr4: 51,980,396-51,980,396 , GRCh38.p12 chr4: 70,158,585-70,158,585 , GRCh38.p12 chr4: 70,159,103-70,159,103 , GRCh37 chr4: 52,846,160-52,846,160 , GRCh37 chr4: 52,846,562-52,846,562 , GRCh37 chr4: 71,024,302-71,024,302 , GRCh37 chr4: 71,024,820-71,024,820 , GRCh38.p12 chr4|NW_013171801.1: 203,171-203,171 , GRCh38.p12 chr4|NW_013171801.1: 203,689-203,689 PRR27
    nsv6296624copy number variation1nstd186human GRCh37 chr4: 70,880,571-70,880,878 , GRCh38.p12 chr4: 70,014,854-70,015,161 , GRCh38.p12 chr4|NW_013171801.1: 54,990-55,297 0
    nsv6293042mobile element insertion1nstd186human GRCh37 chr4: 70,886,885-70,886,885 , GRCh38.p12 chr4: 70,021,168-70,021,168 , GRCh38.p12 chr4|NW_013171801.1: 61,304-61,304 0
    nsv5333150translocation1nstd200human GRCh37 chr4: 70,880,571-70,880,571 , GRCh37 chr4: 70,880,878-70,880,878 , GRCh38.p12 chr4: 70,015,161-70,015,161 , GRCh38.p12 chr4: 70,014,854-70,014,854 , GRCh38.p12 chr4|NW_013171801.1: 55,297-55,297 , GRCh38.p12 chr4|NW_013171801.1: 54,990-54,990 0
    nsv4800131copy number variation1nstd200human GRCh37 chr4: 70,973,780-70,984,226 , GRCh38.p12 chr4|NW_013171801.1: 152,649-163,095 , GRCh38.p12 chr4: 70,108,063-70,118,509 0
    nsv4800130copy number variation1nstd200human GRCh37 chr4: 70,965,664-70,966,162 , GRCh38.p12 chr4|NW_013171801.1: 144,533-145,031 , GRCh38.p12 chr4: 70,099,947-70,100,445 0
    nsv4800129copy number variation1nstd200human GRCh37 chr4: 70,951,302-70,956,449 , GRCh38.p12 chr4: 70,085,585-70,090,732 , GRCh38.p12 chr4|NW_013171801.1: 125,701-130,849 CSN1S2AP
    nsv4768597insertion1nstd186human GRCh37 chr4: 70,958,642-70,958,642 , GRCh38.p12 chr4|NW_013171801.1: 133,056-133,056 , GRCh38.p12 chr4: 70,092,925-70,092,925 0
    nsv4754539insertion1nstd199human GRCh37 chr4: 70,958,645-70,958,645 , GRCh38.p12 chr4|NW_013171801.1: 137,515-137,515 , GRCh38.p12 chr4: 70,092,928-70,092,928 0
    nsv4750714insertion1nstd199human GRCh37 chr4: 70,874,816-70,874,816 , GRCh38.p12 chr4|NW_013171801.1: 49,235-49,235 , GRCh38.p12 chr4: 70,009,099-70,009,099 0
    nsv4725136insertion1nstd186human GRCh37 chr4: 71,007,599-71,007,599 , GRCh38.p12 chr4: 70,141,882-70,141,882 , GRCh38.p12 chr4|NW_013171801.1: 186,468-186,468 CSN1S2BP
    nsv4684953insertion1nstd194human GRCh37 chr4: 70,958,642-70,958,642 , GRCh38.p12 chr4: 70,092,925-70,092,925 , GRCh38.p12 chr4|NW_013171801.1: 133,056-133,056 0
    nsv4674234copy number variation1nstd102humanUncertain significance GRCh37 chr4: 70,618,421-71,083,238 , GRCh38.p12 chr4|NW_013171801.1: 1-236,512 , GRCh38.p12 chr4: 69,752,703-70,217,521 LOC105377269, CSN1S2AP, 12 more genes
    nsv4647835copy number variation1nstd186human GRCh37 chr4: 70,874,773-70,874,872 , GRCh38.p12 chr4|NW_013171801.1: 49,192-49,291 , GRCh38.p12 chr4: 70,009,056-70,009,155 0
    nsv4597438copy number variation2nstd183human GRCh37 chr4: 71,027,612-71,030,602 , GRCh38.p12 chr4|NW_013171801.1: 206,481-209,471 , GRCh38.p12 chr4: 70,161,895-70,164,885 PRR27
    nsv4597437copy number variation1nstd183human GRCh37 chr4: 70,897,472-70,897,784 , GRCh38.p12 chr4: 70,031,755-70,032,067 , GRCh38.p12 chr4|NW_013171801.1: 71,891-72,203 HTN3
    nsv4591464copy number variation1nstd183human GRCh37 chr4: 71,030,071-71,034,918 , GRCh38.p12 chr4: 70,164,354-70,169,201 , GRCh38.p12 chr4|NW_013171801.1: 208,940-213,787 PRR27
    nsv4589134copy number variation2nstd183human GRCh37 chr4: 71,027,455-71,050,560 , GRCh38.p12 chr4|NW_013171801.1: 206,324-229,429 , GRCh38.p12 chr4: 70,161,738-70,184,843 PRR27, LOC105377270
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