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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976783insertion1nstd209human GRCh38 chr19: 54,188,015-54,188,015 , GRCh37.p13 chr19|NW_004166865.1: 162,382-162,382 MBOAT7, TSEN34
    nsv5661192insertion1nstd207human GRCh38 chr19: 54,188,014-54,188,014 , GRCh37.p13 chr19|NW_004166865.1: 162,381-162,381 MBOAT7, TSEN34
    nsv5650716insertion1nstd207human GRCh38 chr19: 54,188,013-54,188,013 , GRCh37.p13 chr19|NW_004166865.1: 162,380-162,380 TSEN34, MBOAT7
    nsv5550540insertion1nstd206human GRCh38 chr19: 54,188,014-54,188,014 , GRCh37.p13 chr19|NW_004166865.1: 162,381-162,381 TSEN34, MBOAT7
    nsv4861337copy number variation1nstd200human GRCh37 chr19: 54,698,654-54,699,104 , GRCh38.p12 chr19|NW_003571057.2: 169,768-170,218 , GRCh38.p12 chr19|NW_003571058.2: 169,768-170,218 , GRCh38.p12 chr19|NW_003571054.1: 169,592-170,043 , GRCh38.p12 chr19: 54,194,796-54,195,246 , GRCh38.p12 chr19|NT_187693.1: 169,768-170,218 , GRCh38.p12 chr19|NW_003571056.2: 169,768-170,218 , GRCh38.p12 chr19|NW_003571061.2: 169,768-170,218 , GRCh38.p12 chr19|NW_003571059.2: 169,768-170,218 , GRCh38.p12 chr19|NW_003571060.1: 169,759-170,210 , GRCh38.p12 chr19|NW_003571055.2: 169,768-170,218 TSEN34
    nsv4861336copy number variation1nstd200human GRCh37 chr19: 54,698,488-54,698,994 , GRCh38.p12 chr19|NW_003571061.2: 169,602-170,108 , GRCh38.p12 chr19|NW_003571059.2: 169,602-170,108 , GRCh38.p12 chr19|NW_003571054.1: 169,426-169,932 , GRCh38.p12 chr19: 54,194,630-54,195,136 , GRCh38.p12 chr19|NW_003571058.2: 169,602-170,108 , GRCh38.p12 chr19|NW_003571060.1: 169,593-170,099 , GRCh38.p12 chr19|NW_003571056.2: 169,602-170,108 , GRCh38.p12 chr19|NW_003571055.2: 169,602-170,108 , GRCh38.p12 chr19|NT_187693.1: 169,602-170,108 , GRCh38.p12 chr19|NW_003571057.2: 169,602-170,108 TSEN34
    nsv4752088insertion1nstd199human GRCh37 chr19: 54,691,896-54,691,896 , GRCh38.p12 chr19: 54,188,014-54,188,014 , GRCh38.p12 chr19|NT_187693.1: 163,010-163,010 , GRCh38.p12 chr19|NW_003571061.2: 163,010-163,010 , GRCh38.p12 chr19|NW_003571057.2: 163,010-163,010 , GRCh38.p12 chr19|NW_003571058.2: 163,010-163,010 , GRCh38.p12 chr19|NW_003571059.2: 163,010-163,010 , GRCh38.p12 chr19|NW_003571060.1: 162,974-162,974 , GRCh38.p12 chr19|NW_003571056.2: 163,010-163,010 , GRCh38.p12 chr19|NW_003571055.2: 163,010-163,010 , GRCh38.p12 chr19|NW_003571054.1: 162,807-162,807 TSEN34, MBOAT7
    nsv4730034copy number variation1nstd102humanUncertain significance GRCh37 chr19: 54,334,195-56,434,037 , GRCh38.p12 chr19: 53,830,941-55,922,671 , GRCh38.p12 chr19|NT_187693.1: 1-1,066,800 , GRCh38.p12 chr19|NW_003571057.2: 1-1,091,841 , GRCh38.p12 chr19|NW_003571058.2: 1-1,066,390 , GRCh38.p12 chr19|NW_003571056.2: 1-1,064,304 KIR3DP1, NLRP9, 133 more genes
    nsv4729999copy number variation1nstd102humanUncertain significance GRCh37 chr19: 54,659,105-54,916,280 , GRCh38.p12 chr19|NT_187693.1: 134,805-387,394 , GRCh38.p12 chr19|NW_003571054.1: 130,217-309,793 , GRCh38.p12 chr19: 54,155,367-54,404,676 , GRCh38.p12 chr19|NW_003571061.2: 130,218-361,078 , GRCh38.p12 chr19|NW_003571060.1: 130,218-309,667 , GRCh38.p12 chr19|NW_003571055.2: 134,805-385,761 RPS9, MIR4752, 23 more genes
    nsv4729755copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,463,931-57,095,254 , GRCh38.p12 chr19: 47,960,674-56,583,886 SIGLEC5, MED25, 574 more genes
    nsv4676386copy number variation1nstd102humanUncertain significance GRCh37 chr19: 54,474,844-55,181,741 , GRCh38.p12 chr19|NT_187693.1: 134,805-652,855 , GRCh38.p12 chr19: 54,071,461-54,670,290 , GRCh38.p12 chr19|NW_003571060.1: 1-575,172 , GRCh38.p12 chr19|NW_003571061.2: 1-396,794 , GRCh38.p12 chr19|NW_003571055.2: 1-394,095 , GRCh38.p12 chr19|NW_003571054.1: 1-576,693 OSCAR, CNOT3, 48 more genes
    nsv4632036copy number variation1nstd183human GRCh37 chr19: 54,693,061-54,693,352 , GRCh38.p12 chr19|NW_003571058.2: 164,175-164,466 , GRCh38.p12 chr19|NW_003571060.1: 164,174-164,465 , GRCh38.p12 chr19|NW_003571056.2: 164,175-164,466 , GRCh38.p12 chr19|NW_003571061.2: 164,175-164,466 , GRCh38.p12 chr19|NT_187693.1: 164,175-164,466 , GRCh38.p12 chr19|NW_003571057.2: 164,175-164,466 , GRCh38.p12 chr19: 54,189,210-54,189,501 , GRCh38.p12 chr19|NW_003571059.2: 164,175-164,466 , GRCh38.p12 chr19|NW_003571055.2: 164,175-164,466 , GRCh38.p12 chr19|NW_003571054.1: 164,007-164,298 MBOAT7, TSEN34
    nsv4626430copy number variation1nstd183human GRCh37 chr19: 54,657,877-54,741,319 , GRCh38.p12 chr19: 54,154,140-54,237,443 , GRCh38.p12 chr19|NW_003571061.2: 128,990-195,632 , GRCh38.p12 chr19|NW_003571059.2: 128,990-195,632 , GRCh38.p12 chr19|NW_003571058.2: 128,990-195,632 , GRCh38.p12 chr19|NW_003571060.1: 128,990-212,432 , GRCh38.p12 chr19|NW_003571056.2: 128,990-195,632 , GRCh38.p12 chr19|NW_003571055.2: 134,805-195,632 , GRCh38.p12 chr19|NW_003571054.1: 128,990-212,219 , GRCh38.p12 chr19|NT_187693.1: 134,805-212,433 , GRCh38.p12 chr19|NW_003571057.2: 128,990-195,632 , LOC107987425, 17 more genes
    nsv4623004copy number variation1nstd183human GRCh37 chr19: 54,681,950-54,723,239 , GRCh38.p12 chr19|NW_003571061.2: 153,064-194,353 , GRCh38.p12 chr19|NW_003571059.2: 153,064-194,353 , GRCh38.p12 chr19|NW_003571055.2: 153,064-194,353 , GRCh38.p12 chr19|NW_003571054.1: 153,022-194,170 , GRCh38.p12 chr19: 54,178,233-54,219,370 , GRCh38.p12 chr19|NT_187693.1: 153,064-194,353 , GRCh38.p12 chr19|NW_003571057.2: 153,064-194,353 , GRCh38.p12 chr19|NW_003571060.1: 153,027-194,356 , GRCh38.p12 chr19|NW_003571058.2: 153,064-194,353 , GRCh38.p12 chr19|NW_003571056.2: 153,064-194,353 , LOC107987425, 10 more genes
    nsv4621672copy number variation2nstd183human GRCh37 chr19: 54,695,874-54,849,275 , GRCh38.p12 chr19: 54,192,023-54,338,004 , GRCh38.p12 chr19|NT_187693.1: 166,988-320,389 , GRCh38.p12 chr19|NW_003571060.1: 166,987-253,362 , GRCh38.p12 chr19|NW_003571055.2: 166,988-319,351 , GRCh38.p12 chr19|NW_003571054.1: 166,820-309,793 , GRCh38.p12 chr19|NW_003571061.2: 166,988-319,505 LAIR1, LILRA5, 19 more genes
    nsv4620576copy number variation1nstd183human GRCh37 chr19: 54,693,784-54,694,236 , GRCh38.p12 chr19|NW_003571058.2: 164,898-165,350 , GRCh38.p12 chr19|NW_003571060.1: 164,897-165,349 , GRCh38.p12 chr19|NW_003571056.2: 164,898-165,350 , GRCh38.p12 chr19: 54,189,933-54,190,385 , GRCh38.p12 chr19|NW_003571061.2: 164,898-165,350 , GRCh38.p12 chr19|NW_003571059.2: 164,898-165,350 , GRCh38.p12 chr19|NW_003571055.2: 164,898-165,350 , GRCh38.p12 chr19|NW_003571054.1: 164,730-165,182 , GRCh38.p12 chr19|NT_187693.1: 164,898-165,350 , GRCh38.p12 chr19|NW_003571057.2: 164,898-165,350 MBOAT7, TSEN34
    nsv4619066copy number variation1nstd183human GRCh37 chr19: 54,693,118-54,695,388 , GRCh38.p12 chr19|NW_003571061.2: 164,232-166,502 , GRCh38.p12 chr19|NW_003571059.2: 164,232-166,502 , GRCh38.p12 chr19|NW_003571054.1: 164,064-166,334 , GRCh38.p12 chr19|NT_187693.1: 164,232-166,502 , GRCh38.p12 chr19|NW_003571058.2: 164,232-166,502 , GRCh38.p12 chr19|NW_003571060.1: 164,231-166,501 , GRCh38.p12 chr19|NW_003571056.2: 164,232-166,502 , GRCh38.p12 chr19|NW_003571057.2: 164,232-166,502 , GRCh38.p12 chr19: 54,189,267-54,191,537 , GRCh38.p12 chr19|NW_003571055.2: 164,232-166,502 MBOAT7, TSEN34
    nsv4383528copy number variation1nstd173human GRCh37 chr19: 54,663,509-54,730,309 , GRCh38.p12 chr19: 54,159,771-54,226,436 , GRCh38.p12 chr19|NT_187693.1: 134,805-201,423 , GRCh38.p12 chr19|NW_003571061.2: 134,622-195,632 , GRCh38.p12 chr19|NW_003571057.2: 134,622-195,632 , GRCh38.p12 chr19|NW_003571058.2: 134,622-195,632 , GRCh38.p12 chr19|NW_003571059.2: 134,622-195,632 , GRCh38.p12 chr19|NW_003571060.1: 134,622-201,421 , GRCh38.p12 chr19|NW_003571056.2: 134,622-195,632 , GRCh38.p12 chr19|NW_003571055.2: 134,805-195,632 , GRCh38.p12 chr19|NW_003571054.1: 134,621-201,236 , LOC107987425, 13 more genes
    nsv4271954copy number variation1nstd166human GRCh37.p13 chr19: 54,688,892-54,704,296 , GRCh38.p12 chr19|NW_003571061.2: 160,006-175,410 , GRCh38.p12 chr19|NW_003571058.2: 160,006-175,410 , GRCh38.p12 chr19|NW_003571060.1: 159,968-175,401 , GRCh38.p12 chr19|NW_003571056.2: 160,006-175,410 , GRCh38.p12 chr19|NW_003571054.1: 159,801-175,228 , GRCh38.p12 chr19|NW_003571059.2: 160,006-175,410 , GRCh38.p12 chr19|NW_003571055.2: 160,006-175,410 , GRCh38.p12 chr19: 54,185,008-54,200,429 , GRCh38.p12 chr19|NT_187693.1: 160,006-175,410 , GRCh38.p12 chr19|NW_003571057.2: 160,006-175,410 TSEN34, RPS9, 1 more genes
    nsv3960776insertion1nstd168human GRCh38 chr19: 54,193,424-54,360,293 , GRCh37.p13 chr19|NW_004166865.1: 167,791-334,660 LILRB3, LILRA4, 13 more genes
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