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Items: 1 to 20 of 2938

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3674459sequence alteration1estd217human GRCh37 chrY: 20,869,231-20,886,812 , GRCh38.p12 chrY: 18,707,345-18,724,926 OFD1P6Y
    esv3674279sequence alteration1estd217human GRCh37 chrX: 62,348,349-62,360,099 , GRCh38.p12 chrX: 63,128,879-63,140,631 LOC105377211
    esv3671802sequence alteration1estd217human GRCh37 chr6: 53,928,709-53,934,829 , GRCh38.p12 chr6: 54,063,911-54,070,031 MLIP
    esv3673661sequence alteration1estd217human GRCh37 chr17: 57,657,447-57,663,173 , GRCh38.p12 chr17: 59,580,086-59,585,812 DHX40
    esv3674471sequence alteration1estd217human GRCh37 chrY: 27,809,025-27,813,823 , GRCh38.p12 chrY: 25,662,878-25,667,676 ELOCP34
    esv3672452sequence alteration1estd217human GRCh37 chr9: 65,913,807-65,917,720 , GRCh38.p12 chr9: 67,545,308-67,549,221 LOC105379452
    esv3674662sequence alteration1estd217human GRCh37 chr1: 24,295,576-24,298,955 , GRCh38.p12 chr1: 23,969,086-23,972,465 SRSF10
    esv3672400sequence alteration1estd217human GRCh37 chr8: 145,433,171-145,436,418 , GRCh38.p12 chr8: 144,133,060-144,136,307 HGH1
    esv3674490sequence alteration1estd217human GRCh37 chr2: 89,962,323-89,965,104 , GRCh38.p12 chr2: 89,923,513-89,926,294 IGK
    esv3674759sequence alteration1estd217human GRCh37 chr3: 75,791,479-75,794,242 , GRCh38.p12 chr3: 75,742,328-75,745,091 ZNF717
    esv3671614sequence alteration1estd217human GRCh37 chr5: 70,239,622-70,242,365 , GRCh38.p12 chr5|NW_003315917.2: 464,253-466,993 , GRCh38.p12 chr5: 70,943,795-70,946,538 , GRCh38.p12 chr5|NT_187651.1: 492,228-494,970 SMN1, GUSBP15
    esv3673392sequence alteration1estd217human GRCh37 chr15: 83,068,823-83,071,460 , GRCh38.p12 chr15: 82,400,087-82,402,724 , GRCh38.p12 chr15|NT_187606.1: 189,178-191,815 UBE2Q2P2
    esv3674357sequence alteration1estd217human GRCh37 chrX: 114,542,522-114,544,514 , GRCh38.p12 chrX: 115,307,957-115,309,949 LUZP4
    esv3674131sequence alteration1estd217human GRCh37 chr22: 21,658,169-21,660,143 , GRCh38.p12 chr22: 21,303,880-21,305,854 FAM230H
    esv3674297sequence alteration1estd217human GRCh37 chrX: 70,569,304-70,571,174 , GRCh38.p12 chrX: 71,349,454-71,351,324 RHOG2P
    esv3673456sequence alteration1estd217human GRCh37 chr16: 16,457,063-16,458,923 , GRCh38.p12 chr16: 16,363,206-16,365,066 , GRCh38.p12 chr16|NT_187607.1: 2,022,395-2,024,255 PKD1P2
    esv3672451sequence alteration1estd217human GRCh37 chr9: 65,780,565-65,782,409 , GRCh38.p12 chr9: 67,412,066-67,413,910 LOC101927602
    esv3673339sequence alteration1estd217human GRCh37 chr15: 41,851,540-41,853,312 , GRCh38.p12 chr15: 41,559,342-41,561,114 TYRO3
    esv3672165sequence alteration1estd217human GRCh37 chr7: 142,360,546-142,362,014 , GRCh38.p12 chr7: 142,653,049-142,654,516 TRB
    esv3672127sequence alteration1estd217human GRCh37 chr1: 147,434,656-147,436,113 , GRCh38.p12 chr1: 147,962,424-147,963,881 GPR89B
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