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Items: 1 to 20 of 2349

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137688copy number variation1nstd102humanBenign GRCh37 chr16: 21,689,835-21,772,050 , GRCh38.p12 chr16: 21,678,514-21,760,729 , GRCh38.p12 chr16|NW_017852933.1: 1,344,051-1,426,323 LOC105371126, OTOA
    nsv6130202insertion1nstd186human GRCh37 chr16: 21,188,665-21,188,678 , GRCh38.p12 chr16: 21,177,344-21,177,357 , GRCh38.p12 chr16|NW_017852933.1: 1,035-1,048 LDAF1
    nsv6122418copy number variation1nstd186human GRCh37 chr16: 21,830,411-21,830,709 , GRCh38.p12 chr16: 21,819,090-21,819,388 , GRCh38.p12 chr16|NW_017852933.1: 1,285,392-1,285,690 RRN3P1
    nsv6120983copy number variation1nstd186human GRCh37 chr16: 21,797,385-21,797,646 , GRCh38.p12 chr16: 21,786,064-21,786,325 , GRCh38.p12 chr16|NW_017852933.1: 1,318,455-1,318,716 LOC105371126
    nsv6120586copy number variation1nstd186human GRCh37 chr16: 22,087,020-22,092,016 , GRCh38.p12 chr16: 22,075,699-22,080,695 , GRCh38.p12 chr16|NW_017852933.1: 1,024,343-1,029,339 MOSMO
    nsv6117432mobile element insertion1nstd186human GRCh37 chr16: 22,019,383-22,019,432 , GRCh38.p12 chr16|NW_017852933.1: 1,096,927-1,096,976 , GRCh38.p12 chr16: 22,008,062-22,008,111 MOSMO
    nsv6115852copy number variation1nstd186human GRCh37 chr16: 22,452,321-22,467,807 , GRCh38.p12 chr16: 22,441,000-22,456,486 , GRCh38.p12 chr16|NW_017852933.1: 648,549-664,040 SMG1P1
    nsv6113315mobile element insertion1nstd186human GRCh37 chr16: 21,239,067-21,239,118 , GRCh38.p12 chr16|NW_017852933.1: 51,437-51,488 , GRCh38.p12 chr16: 21,227,746-21,227,797 LOC105371123
    nsv5980457copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 21,936,726-22,461,225 , GRCh38.p12 chr16: 21,925,405-22,449,904 , GRCh38.p12 chr16|NW_017852933.1: 655,131-1,179,634 CDR2, UQCRC2, 16 more genes
    nsv5345357translocation1nstd200human GRCh37 chr16: 21,629,395-21,629,395 , GRCh37 chr16: 21,636,249-21,636,249 , GRCh38.p12 chr16|NW_017852933.1: 1,486,784-1,486,784 , GRCh38.p12 chr16: 21,618,074-21,618,074 , GRCh38.p12 chr16|NW_017852933.1: 1,479,899-1,479,899 , GRCh38.p12 chr16: 21,624,928-21,624,928 METTL9
    nsv5345014translocation1nstd200human GRCh37 chr16: 22,407,160-22,407,160 , GRCh37 chr16: 21,346,301-21,346,301 , GRCh38.p12 chr16: 21,334,980-21,334,980 , GRCh38.p12 chr16|NW_017852933.1: 158,660-158,660 , GRCh38.p12 chr16: 22,395,839-22,395,839 , GRCh38.p12 chr16|NW_017852933.1: 709,200-709,200 MFSD13B
    nsv5344788translocation1nstd200human GRCh37 chr16: 22,138,368-22,138,368 , GRCh37 chr16: 22,138,314-22,138,314 , GRCh38.p12 chr16: 22,126,993-22,126,993 , GRCh38.p12 chr16: 22,127,047-22,127,047 , GRCh38.p12 chr16|NW_017852933.1: 977,991-977,991 , GRCh38.p12 chr16|NW_017852933.1: 978,045-978,045 VWA3A
    nsv5343991translocation1nstd200human GRCh37 chr15: 44,827,339-44,827,339 , GRCh37 chr16: 21,303,447-21,303,447 , GRCh38.p12 chr15: 44,535,141-44,535,141 , GRCh38.p12 chr16: 21,292,126-21,292,126 , GRCh38.p12 chr16|NW_017852933.1: 115,817-115,817 CRYM, EIF3J, 2 more genes
    nsv5342052translocation1nstd200human GRCh37 chr16: 22,086,806-22,086,806 , GRCh37 chr16: 22,019,729-22,019,729 , GRCh38.p12 chr16: 22,008,408-22,008,408 , GRCh38.p12 chr16: 22,075,485-22,075,485 , GRCh38.p12 chr16|NW_017852933.1: 1,029,553-1,029,553 , GRCh38.p12 chr16|NW_017852933.1: 1,096,630-1,096,630 MOSMO
    nsv5337672translocation1nstd200human GRCh37 chr16: 21,624,158-21,624,158 , GRCh37 chr16: 21,629,184-21,629,184 , GRCh38.p12 chr16: 21,612,837-21,612,837 , GRCh38.p12 chr16: 21,617,863-21,617,863 , GRCh38.p12 chr16|NW_017852933.1: 1,486,995-1,486,995 , GRCh38.p12 chr16|NW_017852933.1: 1,492,005-1,492,005 METTL9
    nsv5335915translocation1nstd200human GRCh37 chr16: 21,623,963-21,623,963 , GRCh37 chr16: 21,611,219-21,611,219 , GRCh38.p12 chr16: 21,612,642-21,612,642 , GRCh38.p12 chr16|NW_017852933.1: 1,504,919-1,504,919 , GRCh38.p12 chr16: 21,599,898-21,599,898 , GRCh38.p12 chr16|NW_017852933.1: 1,492,200-1,492,200 METTL9, LOC101927814
    nsv5333860translocation1nstd200human GRCh37 chr16: 22,399,431-22,399,431 , GRCh37 chr16: 22,397,996-22,397,996 , GRCh38.p12 chr16|NW_017852933.1: 716,929-716,929 , GRCh38.p12 chr16|NW_017852933.1: 718,364-718,364 , GRCh38.p12 chr16: 22,388,110-22,388,110 , GRCh38.p12 chr16: 22,386,675-22,386,675 MFSD13B
    nsv5333641translocation1nstd200human GRCh37 chr16: 22,782,168-22,782,168 , GRCh37 chr16: 21,601,590-21,601,590 , GRCh38.p12 chr16|NW_017852933.1: 1,514,549-1,514,549 , GRCh38.p12 chr16: 22,770,847-22,770,847 , GRCh38.p12 chr16: 21,590,269-21,590,269 LOC101927814
    nsv5332610translocation1nstd200human GRCh37 chr16: 21,707,183-21,707,183 , GRCh37 chr16: 21,707,303-21,707,303 , GRCh38.p12 chr16|NW_017852933.1: 1,408,858-1,408,858 , GRCh38.p12 chr16: 21,695,862-21,695,862 , GRCh38.p12 chr16: 21,695,982-21,695,982 , GRCh38.p12 chr16|NW_017852933.1: 1,408,981-1,408,981 OTOA
    nsv5330428translocation1nstd200human GRCh37 chr16: 21,326,980-21,326,980 , GRCh37 chr16: 21,327,187-21,327,187 , GRCh38.p12 chr16: 21,315,659-21,315,659 , GRCh38.p12 chr16|NW_017852933.1: 139,557-139,557 , GRCh38.p12 chr16: 21,315,866-21,315,866 , GRCh38.p12 chr16|NW_017852933.1: 139,350-139,350 CRYM-AS1
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